Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.
The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.
Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.
Minimum severity
Fresh Take Crave Away Italian Mega sandwiches are recalled due to Listeria monocytogenes detected on food contact surfaces at the manufacturer's facility. The product was distributed across the Southwest and to military facilities.
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Chicken Salad Multigrain Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility.
Fresh & Ready Foods is recalling Roasted Chicken on Wheat Sandwiches (8.5 oz.) because Listeria monocytogenes was detected on food contact surfaces at the manufacturing facility.
Fresh & Ready Foods LLC is recalling Mega Italian Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility.
Fresh & Ready Foods Veggie Snack Bistro Box (4 oz., best buy dates 05/09/2025–05/12/2025) is recalled because Listeria monocytogenes was detected on food contact surfaces at the manufacturing facility.
Fresh & Ready Foods is recalling Chicken Salad on Wheat Sandwiches (4.5oz) due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The affected products were distributed to retailers and military facilities in California, Nevada, Arizona, and Washington.
Fresh & Ready Foods is recalling Turkey & Cheese Multigrain Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The affected product has best-by dates between 05/09/2025 and 05/12/2025.
Fresh & Ready Foods LLC is recalling Almonds & Chocolate Snack 3oz containers due to Listeria monocytogenes detected on food contact surfaces at the manufacturer facility. The product was distributed in the Southwest and to military facilities.
Volvo Trucks North America is recalling 2025-2026 Volvo VN trucks because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.
Portable hook-on chairs sold on Amazon by Ravmix pose a fall hazard because the crotch restraint can be removed without tools, allowing infants to fall through. The product violates federal safety standards. Consumers should stop using immediately and contact Ravmix for refund instructions.
About 3.8 million BowFlex 552 and 1090 adjustable dumbbells are recalled because weight plates can dislodge from the handle during use. Over 100 injuries have been reported, including concussions and broken toes.
ZHORANGE portable bassinets (model 148012-A) are recalled due to sides that are too low and absence of a stand, creating a fall hazard for infants. The product violates federal safety standards for infant sleep products.
Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.
NTI Boilers is recalling about 323 NTI-brand TRX Series II residential wall-mounted gas boilers sold in the US because the boiler door can fail to seal properly, posing fire and carbon monoxide poisoning hazards that can result in death or serious injury.
About 380 Funlio convertible high chairs pose entrapment and fall hazards due to violations of federal safety standards. The opening between seat and tray is large enough for a child to become trapped, and the child restraint system can fail.
HTP-brand ELU Elite Ultra residential gas boilers are being recalled because the boiler door can fail to seal properly, allowing flames and gases to escape, posing fire and carbon monoxide poisoning hazards that can result in death or serious injury.
ZRWD infant swings (model S0008A) sold on Amazon are recalled due to suffocation risk from incline angles exceeding safety limits and missing battery hazard warnings. About 3,540 units are affected.
Starcraft RV is recalling 45 units of the 2025 Autumn Ridge travel trailer because undersized safety chains could fail, allowing the trailer to separate from the tow vehicle.
Honda is recalling certain 2025 CR-V Hybrid vehicles because the fuel feed hose may have been improperly installed, allowing fuel to leak. This fails FMVSS 301.
Triple E is recalling 2025 Wonder and Unity motorhomes because incorrectly installed inverter wiring insulation may overheat, increasing the risk of fire.
Glenmark Pharmaceuticals is recalling Carvedilol Tablets USP 25 mg nationwide due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from CGMP deviations.
Onkos Surgical is recalling ELEOS Collar Stem components (Model HC-15120-03M) that were packaged and labeled as 13mm modular segmental stems when they are actually 15mm in diameter. This mislabeling could result in implantation of an incorrectly-sized component during limb salvage surgery.
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 12.5 mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit, resulting from current Good Manufacturing Practice (CGMP) deviations.
Onkos Surgical is recalling 23 units of ELEOS Collar Stem implants (Model HC-13120-03M) because packages labeled as 13mm contained 15mm diameter implants instead, creating a risk of implant mismatch during surgery.
Glenmark Pharmaceuticals Inc., USA is recalling Carvedilol Tablets USP 3.125mg due to the presence of N-Nitroso Carvedilol I impurity above the recommended acceptable intake limit. The recall affects 100-count and 500-count bottles distributed nationwide.