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
AVID Medical, Inc. is recalling Halyard convenience kits containing Medline Namic Angiographic Star Off Handle Manifolds because particulates may be present in the fluid path.
HEAD Watersports is recalling Apeks second stage scuba regulators because they can restrict airflow at depths exceeding 45 meters, posing a risk of serious injury or death.
A2batt is recalling EEMB Lithium-ion Coin Battery Chargers because the included batteries can be easily accessed by children, posing a risk of serious injury or death if swallowed.
PIXLABBY is recalling its silicone magnetic fidget sliders because they can release high-powered magnets that pose a serious injury or death risk if swallowed by children.
BUSOHA is recalling approximately 2,186 Magnetic Fidget Slider Toys sold on Amazon because they can release magnets that pose a serious injury or death risk if swallowed.
Wichard Groupe North America is recalling Courant Spliced Kalimba climbing ropes because the spliced ends can fail, creating a risk of serious injury or death from falls.
Medical Action Industries is recalling cardiovascular procedure kits containing manifolds that may have particulate in the fluid path, which could enter blood circulation and lodge in blood vessels. FDA Class I.
ResMed is recalling Astral 100/150 ventilators because supercapacitor electrolyte leakage can damage the charger chip, trigger a fail-safe state, and interrupt ventilation therapy.
Nelson & Isa Lacteos LLC is recalling 480 1-lb packages of Requeson soft ricotta sold in NY because the product may be contaminated with Listeria monocytogenes.
About 121,680 Galanz retro-style refrigerators can short circuit and ignite. CPSC is aware of 34 fire reports, one of which resulted in a fatality. Free in-home repair is offered.
About 1.5 million OCOOPA lithium-ion hand warmers can overheat and ignite. The firm reports 1,480 overheating incidents, 15 fires and 350 burn injuries, including the death of an 83-year-old consumer.
JB Chemicals and Pharmaceuticals Ltd is recalling 34,020 bottles of Cetirizine Hydrochloride Tablets USP 5 mg because some tablets were found to contain Ranitidine due to cross contamination.
Medline Industries, LP is recalling specific C-Section convenience kits because they contain Bupivacaine Hydrochloride in Dextrose Injection, USP, which is subject to a voluntary recall due to quality issues.
Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.
Junpower CR2032 Batteries (20-piece packs) lack required child-resistant packaging and warning labels. If swallowed, these lithium coin batteries can cause serious internal injuries or death.
KayserBett IDA pediatric care beds are being recalled because the hand control can be operated by children, creating a risk of entrapment and serious injury or death.
Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.
MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.
Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.
EEMB lithium coin battery packs sold online are not in child-resistant packaging as required by law. If swallowed by a child, these batteries can cause serious internal injuries or death.
OmniDose is recalling 23,000 lithium battery packs used in its X4 insulin pumps after reports of unexpected shutdown.
AMZCMJ DGD is recalling its children's tower stools because they can tip over or collapse, posing risks of serious injury or death from falls and entrapment.