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
About 450 two-packs of Joly's 80% Vinegar are being recalled because the hazardous substance lacks required warning labels and first-aid treatment instructions.
About 3,295 SAMIT youth multi-purpose helmets are being recalled because they do not comply with the positional stability and certification requirements of the bicycle helmet standard.
McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.
Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.
Costco Wholesale is recalling 8,073 packages of Kirkland Signature Mini Beignets filled with Caramel over undeclared hazelnut.
Carrot Top Kitchens is recalling 12 units of Lime Ginger Hummus, 8 oz, because it contains undeclared sesame.
Carrot Top Kitchens is recalling 12 units of Sundried Tomato and Caper Hummus, 8 oz, because it contains undeclared sesame.
Medline is recalling 48 reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
Carrot Top Kitchens is recalling 12 units of Cherry Pepper Hummus, 8 oz, because it contains undeclared sesame.
Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.
Carrot Top Kitchens is recalling 12 units of Lemon & Garlic Hummus, 8 oz, because it contains undeclared sesame.
Medline is recalling 311 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 41 reprocessed Livewire steerable diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
Carrot Top Kitchens is recalling 12 units of White Truffle Hummus, 8 oz, because it contains undeclared sesame.
Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 228 units because these lots of reprocessed catheters may contain small particles of residual material.
Asteria Health is recalling 89,074 pellets of Testosterone, 25.0 mg sterile pellets over the potential presence of metal particulate matter.
AVID Medical is recalling 1,500 Halyard Transport Bag Kits because a Tyvek bag seal issue may compromise the sterility of the kit.
Karison Foods & Snacks is recalling 230 cases of Karison brand Alsi Pinni, 12 oz, because the product contains milk which is undeclared in the ingredient statement.
Intuitive Surgical is recalling 47 da Vinci 5 Surgeon Console Viewer Displays manufactured with outdated firmware, which may cause loss of the 3D surgical field or complete visualization loss.
Hologic is recalling 681,870 Brevera Breast Biopsy System disposable 9 gauge needles because particulates in affected devices can be deposited into breast tissue during use.
Fresenius Kabi Compounding is recalling 1,578 bags of Vancomycin HCl injection over a lack of assurance of sterility.
Fresenius Kabi Compounding is recalling 1,057 bags of acyclovir sodium 200 mg in 100 mL sodium chloride injection over a lack of assurance of sterility.
Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.