Official regulatory feed
3M Company Recalls Scotch™ Thermal Laminators Due to Risk of Serious Injury or Death from Fire Hazard
The recalled thermal laminators can overheat, posing a fire hazard.
Official-source monitor
Live mass tort news and product safety alerts.
Current government recalls, drug and device safety communications, public-health notices and enforcement releases—clearly labeled and linked to the original source.
Checked hourlyIndividual agencies control their own publication schedules and availability.
A headline is a signal, not proof. An official recall or safety notice can justify investigation and medical follow-up, but it does not establish that a product caused an individual injury or that a lawsuit exists.
RegulatorsFDA and CPSC recalls, warnings and safety communications
Public healthCDC releases involving outbreaks, exposures and injury prevention
EnforcementOSHA and DOJ releases involving unsafe products or conduct
Latest official items
Regulatory and government feed
Official regulatory feed
HatsanUSA Recalls Blitz Air Rifles Due to Risk of Serious Injury or Death from Projectile Hazard
The recalled air rifles can fire unexpectedly when releasing the bolt before the air rifle is fully cocked, posing a risk of serious injury or death from projectile hazard.
Official regulatory feed
Loving Thyself Rocks Recalls Crystal Glass Cups Due to Risk of Serious Injury from Ingestion and Laceration Hazards
Glass can break inside the recalled cups while in use, posing a risk of serious injury from ingestion and laceration hazards.
Official regulatory feed
Papablic, of USA Recalls Convertible Bedside Sleepers Due to Risk of Serious Injury or Death from Entrapment, Suffocation and Fall Hazards; Violate Mandatory Standard for Play Yards
The bedside sleepers with play yard extensions violate the mandatory safety standard for play yards because the mattress can become displaced causing a baby to become entrapped between the sleeping pad and bottom posing a deadly suffocation hazard. In addition, the latching and locking mechanism can fail, causing
Official regulatory feed
Primark Recalls 101 Dalmatians Faux Leather Children’s Coin Purses Due to Phthalate Levels and Risk of Ingestion
The coin purses contain higher phthalate concentration levels. Phthalates can be harmful if young children are exposed to sufficient amounts, including through ingestion, and certain phthalates have been associated with adverse health effects, particularly effects on development and the hormone system.
Official regulatory feed
usOpal Recalls Xalirium Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The b
Official regulatory feed
FDA Launches the Rare Disease Framework Initiative to Develop a Holistic, Fit-For-Purpose Framework for Rare Disease Drug Development
The U.S. Food and Drug Administration, a division within the U.S. Department of Health and Human Services (HHS), today announced the Rare Disease Framework Initiative to reimagine the development of drugs and biologics for rare diseases.
Official regulatory feed
FDA Approves First Treatment for Certain People With BCG-Unresponsive Bladder Cancer
FDA Approves First Treatment for Certain People With BCG-Unresponsive Bladder Cancer
Official regulatory feed
Convenience Kit Recall: AVID Medical Removes Convenience Kits Affected by BD ChloraPrep Applicator Recall
Avid Medical is removing certain convenience kits affected by the BD ChloraPrep Applicator Recall that may be contaminated with Aspergillus penicillioides.
Official regulatory feed
Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter
FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 13, 2026 – Par Health is recalling 22 lots of Argatroban Injection 250 mg/2.5 mL (100 mg/mL) to the hospital/user level. This recall is being conducted due to the presence of particulate matter, identified as cellulose, polystyrene, polyethylene terepht
Official regulatory feed
Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets
BD Alaris Pump Infusion Sets are being removed and discontinued; Alaris Pump Module model 8100 has updated performance data
Official regulatory feed
Convenience Kit Recall: Medline Removes Convenience Kits Affected by BD ChloraPrep Applicator Recall
Certain Medline convenience kits containing recalled BD ChloraPrep applicators should be removed from use due to potential fungal contamination
Official regulatory feed
Krasnyi Oktyabr Inc. Recalls Starfish Seafood Trio Because of Possible Health Risk
Krasnyi Oktyabr Inc. of Brooklyn, New York, is voluntarily recalling Starfish Seafood Trio – Cold Smoked Salmon, Halibut, and Trout, 8 oz (227 g) packages, because the product has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal in
Official regulatory feed
Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter
FOR IMMEDIATE RELEASE - ROCHESTER, MI– October 8, 2026 –Par Health is voluntarily recalling two lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose.
Official regulatory feed
Gardeners Basics Recalls Waltham 29 Broccoli Sprouting Seeds Due to Possible Salmonella Contamination
October 8, 2026, Gardeners Basics of Spanish Fork, Utah, is recalling one-pound bags of broccoli sprouting seeds because they may be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened i
Official regulatory feed
Giant Bicycle Recalls LED-Light Keys Included with SureLock Bike Lock Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
The LED-light key that was included with certain SureLock Bicycle Lock sets violates the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard. Additionally, the packaging and product do not have th
Official regulatory feed
DR Power Equipment Recalls Pilot and Premier Trimmer Mowers Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Grass and debris can accumulate in the trimmer mowers and ignite, posing a risk of serious injury or death from fire and burn hazards.
Official regulatory feed
Decathlon America Recalls Van Rysel GRVL AF Bicycles Due to Risk of Serious Injury or Death from Crash Hazard
The recalled bicycles’ front lock nut can loosen during use, causing the front wheel to dislodge or loosen over time, posing a crash hazard.
Official regulatory feed
ONTHEWEI Recalls Baby Bath Seats Due to Risk of Serious Injury or Death to Children from Drowning; Violate Mandatory Standard for Infant Bath Seats
The recalled bath seats violate the mandatory standard for infant bath seats because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
Official regulatory feed
Pacearth Direct Recalls PACEARTH Swing Seats Due to Risk of Serious Injury from Fall Hazard
The seats, metal carabiners or quick links, or webbing straps of the recalled swing seats can break during use, posing a risk of serious injury due to fall hazard.
Official regulatory feed
Romorgniz Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the STURDY Act .
Official regulatory feed
Snow Peak Recalls Propane Fireplace Inserts and Lava Rocks Due to Risk of Serious Injury or Death from Burn and Fire Hazards
The fireplace’s lava rocks can ignite and explode when heated in the propane insert, posing a risk of serious injury or death from burn and fire hazards.
Official regulatory feed
The Conqueror Recalls Avengers Medals Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Magnets
The recalled medals violate the mandatory safety standard for magnets because the high-powered magnets may detach, posing a deadly ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can
Official regulatory feed
Eden Brothers Recalls Calabrese Broccoli Seeds Due to Possible Salmonella Contamination
Arden, NC – October 7th 2026 – Eden Brothers LLC is recalling Calabrese Broccoli Seeds in Packet, 1 Ounce and 1 Pound sizes (Eden Brothers lots 1022067 and 1022068; supplier lot W4105) because we were informed by our supplier that they may be contaminated with Salmonella.
Official regulatory feed
Pacific Health Sciences Voluntarily Recalls One Lot of Babies' Magic Tea Brand Baby Sleep Gripe Water Dietary Supplement
Pacific Health Sciences is voluntarily recalling one lot of Babies' Magic Tea brand Baby Sleep Gripe Water dietary supplement.
Official regulatory feed
Leader Formulas, LLC. Issues Voluntary Nationwide Recall of RAPTURE Preworkout Due to the Presence of 1,3-Dimethylamylamine (DMAA)
Leader Formulas, LLC. of Tomball, TX, is voluntarily recalling one (1) lot of RAPTURE Pre workout, a dietary supplement powder because it was found to contain 1,3-Dimethylamylamine (DMAA) and sold at the consumer level. Using DMAA can result in elevated blood pressure and could lead to cardiovascula
Official regulatory feed
Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter
WALTHAM, Mass., October 5, 2026 – Nova Biomedical initiated a global Medical Device Correction on July 24, 2026, for the StatStrip® Glucose Hospital Meter System due to a software issue that may cause a glucose result to be associated with the wrong patient. When a patient ID barcode is scanned, pri
Official regulatory feed
FDA Seeks Public Input to Support Ibogaine Research
The U.S. Food and Drug Administration today announced a request for information (RFI) describing approaches the agency is considering for the design of early-phase clinical trials of ibogaine drug products and seeking public input on those approaches.
Official regulatory feed
IV Tubing Set Correction: ICU Medical Updates Use Instructions for IV Tubing Sets
Black specks and particulate reported in drip chambers of certain ICU Medical IV tubing sets does not affect device safety, performance, or intended use.
Official regulatory feed
Stewart’s Shop Corp. Recalls Heavenly Medley and Vanilla-Chocolate-Strawberry Due to Possible Foreign Object
October 2, 2026, Stewart’s Shops Corp. of Saratoga Springs, NY is recalling two flavors, Heavenly Medley and Vanilla-Chocolate-Strawberry, of half-gallon ice cream due to the potential presence of metal.
Official regulatory feed
EAK Distribution LLC Recalls HOME GROWN Green Sprouting Calabrese Broccoli Seeds, 8 oz, Heirloom Because of Possible Health Risk
October 2nd, 2026 - EAK Distribution of Casper, WY is recalling HOME GROWN Green Sprouting Calabrese Broccoli Seeds, 8 oz, Heirloom, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly
Official regulatory feed
Frutas y Hortalizas del Sur S.A. Expands Recalls to Include Additional Lots of Great Value Frozen Organic Triple Berry Blend 10 OZ, Great Value Frozen Organic Blueberries 10 OZ and One Lot of Trader Joe’s Frozen Organic Mixed Berry Blend 12 OZ Because of Potential Contamination with E. coli O145
October 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its previously initiated recalls on July 3, 2026 and September 3,2026 recall of frozen organic IQF blueberries and berry blends to include additional lots of Great Value frozen Organic Triple Berry Blend 10 OZ, Great Value
Official regulatory feed
Breathing Circuit Recall: Draeger Removes VentStar Resus Neo Hoses
Removal of VentStar Resus Neo hoses due to the potential for cracks resulting in restricted ventilation or delayed therapy.
Official regulatory feed
WinCo Foods of Boise, ID is Recalling the Following Salsa Bean Dip Trays Due to the Inclusion of Recalled Peperoncini from G.L. Mezzetta
October 1, 2026 - WinCo Foods of Boise, ID is recalling the following Salsa Bean Dip Trays due to the inclusion of ecalled peperoncini from G.L. Mezzetta.
Official regulatory feed
FDA Approves First Heart Valve Designed to Grow with Children
The U.S. Food and Drug Administration today approved the Autus Size-Adjustable Valve, a surgically implanted pulmonary heart valve for pediatric patients with congenital pulmonary valve disease.
Official regulatory feed
Greenwich Rx Issues Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels
IMMEDIATE RELEASE - Tomball, Texas – October 1, 2026 – Greenwich Rx, a 503A compounding pharmacy, is voluntarily recalling specific lots of its compounded glutathione to the consumer level. The product is being recalled due to potential elevated endotoxin levels.
Official regulatory feed
Gias Foods, Inc. Recalls Bettergoods Authentic Italian Lemon Alfredo Fettuccine Because of Possible Health Risk
Gias Foods of New York, NY is recalling all lot codes of bettergoods Authentic Italian Lemon Alfredo Fettuccine, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people,
Official regulatory feed
Saint Francis Apizza LLC Issues a Voluntary Recall of its Frozen Pizzas for Missing Sub Ingredients on the Label for Soy Which Includes Soybean Oil and Soy Lecithin, an Allergen
Cincinnati, Ohio October 1, 2026. Saint Francis Apizza LLC is issuing a voluntary recall on their frozen pizzas for misbranding due to the soy allergen not being declared on the label. The frozen pizzas were sold in ‘Pepperoni,’ ‘Plain Cheese,’ ‘Supreme,’ and ‘Mushroom and Onion’ varieties.
Official regulatory feed
ABC Trading Recalls Squishy Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
The squishy toys violate the mandatory safety standard for toys because the water beads inside the toys expand larger than permitted, posing a deadly ingestion hazard. If a water bead is ingested, it can pose ingestion, choking, and intestinal obstruction hazards inside a child’s body, resulting in severe discomfort, v
Official regulatory feed
Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard
The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard.
Official regulatory feed
YunHeng Recalls LandTale Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard
Official regulatory feed
LLK Trading Recalls Mochi Malrang Mystery Dumpling Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
The mystery dumpling toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard. If a water bead is ingested, it can pose ingestion, choking, and intestinal obstruction hazards inside a child’s body, resulting in severe
Official regulatory feed
Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards
When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn hazards.
Official regulatory feed
GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. T
Official regulatory feed
Gobi Heat Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
Official regulatory feed
Walmart Recalls Over 4.4 Million Expert Grill Brushes Due to Ingestion Hazard
Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
Official regulatory feed
Kobayashi Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
Official regulatory feed
Dollar Tree Stores Recalls Electric Balloon Pumps Due to Burn Hazard
The recalled electric balloon pumps can overheat, posing a burn hazard.
Official regulatory feed
Golden Resale Recalls Portable Camping Showers Due to Risk of Serious Injury or Death from Fire Hazard
The recalled camping showers’ immersion heaters can quickly ignite when they are partially or completely out of water, posing a risk of serious injury or death from a fire hazard.
Official regulatory feed
Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do
Official regulatory feed
FDA Launches Nationwide Effort to Expand Scientific Expertise and Consumer Voices to Advisory Committees
The U.S. Food and Drug Administration today announced a broad, nationwide recruitment effort to expand the range of qualified voices and perspectives on its advisory committees— the independent bodies that inform some of the most consequential decisions in American public health.
Official regulatory feed
FDA Investigation Leads to Charges Against Two Indian Nationals Involved in Transnational Counterfeit Drug Distribution Scheme
The U.S. Attorney’s Office for the Middle District of Florida and the Criminal Division of the U.S. Department of Justice today announced federal charges against Swapnadip Roy, 33, and Vicky Ramancha, 37, both Indian nationals.
Official regulatory feed
FDA Approves First Treatment for MCT8 Deficiency
The U.S. Food and Drug Administration today approved Emcitate (tiratricol) tablets for oral suspension to treat peripheral thyrotoxicosis (excess thyroid hormone levels in the blood that causes symptoms, such as rapid heart rate, increased blood pressure and adverse effects on metabolism) in patient
Official regulatory feed
FDA intends to evaluate changes to the PMTA regulatory framework
FDA is carefully reviewing its experience implementing the Premarket Tobacco Product Application (PMTA) rule, as well as recent judicial developments, including a federal lawsuit filed in the U.S. District Court for the Northern District of Texas challenging the current regulatory framework.
Official regulatory feed
Sierra Nevada Cheese Company Recalls Graziers Raw Milk Cheese Because of Possible Health Risk
Sierra Nevada Cheese Company of Willows, California, is voluntarily recalling all Graziers Raw Milk Cheese currently in the market because due to potential contamination with Escherichia coli O26:H11 (E. coli O26:H11).
Official regulatory feed
Angiographic Catheter Recall: Boston Scientific Removes Imager II Angiographic Catheters
Boston Scientific Imager II Angiographic Catheters removed due to a manufacturing issue leading to tip detachment; could result in procedural delays, embolism
Official regulatory feed
Heart Pump Controller Recall: Abiomed Removes Automated Impella Controllers
Abiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical circulatory support.
Official regulatory feed
Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing Recalled Sodium Chloride Ampules
BD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampules
Official regulatory feed
ZCK01 Recalls Kesyup Mattresses Due to Risk of Serious Injury or Death from Fire Hazard; Violate Mandatory Standard for Mattress Flammability
The recalled mattresses violate the mandatory flammability standard for mattresses , posing a risk of serious injury or death from fire.
Official regulatory feed
5Color Recalls Children’s Bicycle Helmet and Pads Sets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets
The helmets in the recalled sets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, retention system, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious ri
How to read a live product-safety feed
Recalls, warnings, investigations and lawsuits are different events.
A recall removes, corrects or warns about a product under a regulator's framework. It may be voluntary, company-initiated, requested by an agency or mandated under particular legal authority. Recall classifications generally describe the level of potential health risk; they do not decide whether a person has a civil product-liability claim. Some corrections update software, instructions or monitoring without requiring a device already in a patient to be removed. Read the affected model, lot, batch, serial number and action instructions before assuming a notice applies.
A safety communication can address an emerging signal while an agency collects more data. Passive adverse-event systems are valuable for detecting patterns, but reports can be incomplete, duplicated or unverified and cannot usually calculate how often an injury occurs. A public-health outbreak investigation uses epidemiology, laboratory analysis and traceback to identify a source; its case definition and current count may change as records are reviewed. An enforcement release reports allegations, charges, a plea, judgment or settlement under a government case and should be read for its procedural posture.
Why this feed uses official sources.
Law-firm blogs and commercial news can identify issues worth researching, but republishing their headlines would mix marketing with primary evidence. This public feed is limited to government sources whose releases can be linked directly and dated. Google News search RSS is intentionally excluded because its feed terms describe personal, non-commercial feed-reader use; LawIntaker is a commercial intake site. Commercial reporting may still lead an editor to verify a development against a court filing or agency release before adding it to an evergreen guide.
Official does not mean infallible or final. Agencies update investigations, companies expand recalls, courts change orders and scientific conclusions develop. The feed checks each source hourly, but the publication date shown is the agency's date, not the time LawIntaker fetched it. If one feed is unavailable, the rest continue loading. The direct-source links remain available so readers can verify the latest instructions.
What to save when an alert may apply.
Preserve the label, packaging, receipt, prescription bottle, device card, serial number, batch code, model, lot and photographs. For installed devices, ask the hospital for the operative report and implant stickers. For medicines, request a pharmacy dispensing history showing the manufacturer and National Drug Code when available. For food or consumer products, write down purchase location, dates of use and who used the item. Do not discard a product simply because a retailer offers a refund if an injury may have occurred; obtain medical and legal advice about safe preservation first.
Record symptoms, medical contacts and treatment without guessing at causation. Seek appropriate care and follow the regulator's and clinician's instructions. Do not stop a prescription or implanted therapy solely because of a headline. Some FDA notices expressly warn that stopping treatment can present greater risk than continuing until a clinician identifies an alternative.
When an alert becomes a mass tort.
Many recalls never produce mass litigation. A mass tort generally requires a recurring injury theory, common evidence about a product or conduct, enough viable individual claims and a legal path through jurisdiction, causation and deadlines. Related federal cases may eventually be centralized in an MDL, but centralization is a procedural decision rather than a merits ruling. State cases, consolidated state proceedings, bankruptcy claims or individual suits may exist without a federal MDL.
The LawIntaker mass-tort directory adds a case guide only when public information supports a meaningful litigation or emerging-claim explanation. Each guide states whether the matter is active, emerging, advanced or in a settlement phase; identifies the court source; explains the alleged injury and competing scientific context; and lists records that can verify a screening. The directory does not create a new “lawsuit” from every agency headline.
Submitting an intake is not filing a claim.
A confidential intake can help route facts to an attorney or legal team, but it does not file a complaint, enroll anyone in a settlement, preserve a product or stop a statute of limitation. Representation exists only after a law firm accepts the matter in writing. If an alert appears connected to a serious diagnosis or urgent deadline, seek medical care and prompt advice from a qualified lawyer rather than waiting for another feed update.