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
Philips North America is recalling 24 units of the Ingenia 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Aju Pharm is recalling 416 units of the AlternatiV+ Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.
Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.
Gold Star Distribution is recalling first aid kits and bandages over potential exposure of rodents and rodent activity in its distribution center.
Philips North America is recalling 1 unit of the Evolution Upgrade 3.0T MR system because exported MR Elastography stiffness maps may show stiffness value errors.
Prima Vera Nueva is recalling 9,656 packages (4 tamales per package) of Roasted Pumpkin & White Cheddar Tamales over potential contamination with Listeria monocytogenes.
Aju Pharm is recalling 200 units of the Genesis Push-In Suture Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.
Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.
Medline is recalling 117 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Medline is recalling 236 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Canon Medical Systems is recalling 98 units of the Alphenix INFX-8000F because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Cerapedics is recalling 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft, 1.0cc, over an incorrect expiration date.
Zimmer Surgical is recalling 206 A.T.S. 5000TS Tourniquet Systems because the user interface may freeze or become unresponsive to touch in certain non-English language settings.
Medline is recalling 40 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Medline is recalling 60 units of the Head Shave-Latex Safe Kit because it contains MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked.
Miach Orthopaedics is recalling 284 BEAR Implants because the label carries an expiration date that extends beyond the product's documented and approved shelf life.
CareFusion is recalling 189 BD Alaris Pump Modules, model 8100, because modules flashed with a daylight saving time timestamp may lose connectivity to hospital networks.
Zimmer Surgical is recalling 51 A.T.S. 3200TS Tourniquet Systems because the user interface may freeze or become unresponsive to touch in certain non-English language settings.
Canon Medical Systems is recalling 3 units of the Alphenix INFX-8000H because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
Elekta is recalling 5,391 medical linear accelerators, covering Elekta Synergy, Harmony, Infinity and Versa HD, due to a manufacturing issue and electrical grounding of systems.
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
LimFlow, Inc. is recalling 33 units of the LimFlow Vector, model VT-US-23, over an incorrect expiration date.