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 the agency’s own highest classification or reported deaths or serious injuries, 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
Mako Surgical Corporation is recalling 39 units of the 2.7 Degree Angled Sagittal Saw attachment because the bearings were ungreased.
Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date listed by Lidstock.
Arrow International Inc. is recalling 105 units of Arrow PICC Kits due to incorrect expiration dates on the packaging.
Zimmer Biomet is recalling 313 Mobi-C 14mm Distraction Screws because they were incorrectly labeled as 12mm length screws.
Arrow International Inc is recalling 20 units of Arrow PICC with Chlorag+ard Technology due to an incorrect expiration date on the label.
Arrow International Inc is recalling 983 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates.
Stryker GmbH is recalling 1,600 Endotrac EPF/EGR Hook/Triangle Blade Kits because the sterile bag seal integrity may be compromised.
Arrow International Inc is recalling 48 units of Arrowg+ard Blue Advance PICC catheters because the product has an incorrect expiration date.
Arrow International Inc. is recalling Arrow JACC devices with Chloraguard Technology due to an incorrect expiration date on the packaging.
Mako Surgical Corporation is recalling 2.7 Degree Straight Sagittal Saw attachments because the bearings were ungreased. The devices were distributed to facilities in 13 US states and three international countries.
Arrow International Inc. is recalling 66 units of Arrow PICC powered by Arrow VPS Stylet because the product has an incorrect expiration date.
Arrow International Inc is recalling 108 units of Arrow PICC with Chloraguard Technology because the product was labeled with an incorrect expiration date.
Arrow International Inc is recalling 1,840 units of Arrow PICC Kits because the product labels display an incorrect expiration date.
CooperSurgical is recalling 19 LEEP Precision Integrated Systems because incorrect fuses may have been installed in the generator.
Arrow International Inc. is recalling 9 units of Arrow JACC with Chloraguard Technology due to incorrect expiration dates on the product.
Arrow International is recalling 350 units of Arrowg+ard Blue Advance PICC catheters because the product labels display an incorrect expiration date.
Arrow International Inc is recalling 279 units of Arrowg+ard Blue Advance PICC catheters because the products display an incorrect expiration date.
Arrow International Inc is recalling 2 units of Arrow JACC with Chloraguard Technology due to an incorrect expiration date on the product label.
Arrow International Inc. is recalling 190 units of Arrow PICC Kits due to incorrect expiration dates printed on the product.
Arrow International Inc is recalling 78 units of Arrowg+ard Blue Advance JACC due to incorrect expiration dates. The recall is nationwide.
Arrow International Inc is recalling Arrowg+ard Blue Advance Midline devices due to an incorrect expiration date printed on the product.
Arkray Factory USA, Inc. is recalling 159 AUTION HYBRID AU-4050 units due to a software issue that could assign incorrect patient information to sample results.
Arrow International Inc is recalling 450 units of Arrowg+ard Blue Advance PICC devices due to incorrect expiration dates.
Arrow International Inc. is recalling 52 units of Arrowg+ard Blue Advance JACC products due to an incorrect expiration date.
Arrow International Inc is recalling Arrowg+ard Blue Advance PICC catheters because the product has an incorrect expiration date.