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
Arrow International Inc is recalling 191 units of JACC central catheters because the expiration date printed on the product is incorrect.
Arrow International Inc is recalling 100 units of Arrow PICC Kits due to an incorrect expiration date printed on the product.
Arrow International Inc is recalling 180 units of Arrow PICC with Chlorag+ard Technology because the products bear an incorrect expiration date.
Arrow International Inc. is recalling 162 units of Arrowg+ard Blue Advance PICC catheters due to an incorrect expiration date printed on the product.
Arrow International Inc is recalling 84 units of Arrowg+ard Blue Advance JACC due to incorrect expiration dates.
Arrow International is recalling 159 units of Arrow PICC catheters because the expiration date printed on the packaging is incorrect.
Arrow International is recalling 991 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates on the product.
Arrow International Inc is recalling 185 units of Arrow PICC with Chloraguard Technology due to incorrect expiration dates on the packaging.
Arrow International Inc. is recalling 77 units of Arrowg+ard Blue Advance JACC products because they were labeled with an incorrect expiration date.
Arrow International Inc. is recalling Arrow PICC with Chloraguard Technology due to an incorrect expiration date on the product.
Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date. The recall involves 174 units distributed nationwide.
Arrow International Inc. is recalling 135 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.
Arrow International Inc is recalling 578 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.
Cytocell Ltd. is recalling Aquarius D13S319 Plus Deletion Probes because the chromomap on the package insert contains an error.
Arrow International Inc is recalling 16 units of Arrowg+ard Blue Advance JACC because the product has an incorrect expiration date.
Arrow International Inc. is recalling 12 units of JACC central catheters because the expiration date printed on the packaging is incorrect.
Arrow International Inc. is recalling 6 units of Arrow JACC Central Catheters because the expiration date is incorrect.
Microbiologics Inc is recalling 22 units of the Cepheid Xpert C. difficile/Epi Control Panel because the expiration date is incorrectly labeled as 2021-10-31 instead of 2021-03-31.
Arrow International Inc. is recalling 3 units of Arrow JACC with Chloragard Technology due to an incorrect expiration date.
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices because the balloon may rupture during cardiopulmonary bypass, potentially obscuring the operative site and requiring a change in surgical strategy.
GE Healthcare is recalling 825 Proteus XR/a radiographic systems because a monitor fell off its wall mount due to product aging.
GE Healthcare is recalling 825 Silhouette VR systems because a CRT monitor fell off its wall mount due to product aging.
Conformis, Inc. is recalling 128 iTotal Hip Replacement System stems due to a 3mm discrepancy between approved and manufactured neck/head lengths.
Skytron is recalling five Integrity 270 Steam Sterilizers because the weld attaching the air heater assembly has shown signs of fatigue or failure.
GE Healthcare is recalling 825 Prestilix 1600X digital radiology systems because a monitor fell off its wall mount due to product aging.