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
Cardinal Health is recalling 3,507 Jackson-Pratt Channel Drains (19 Fr) due to performance defects including lack of radiopacity, dull trocars, lack of flexibility, and broken tips. Drains were distributed worldwide.
Cardinal Health Jackson-Pratt Channel Drains (19 Fr, REF JP-2230) are recalled due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips affecting 29,515 units.
Superior Fresh LLC is recalling Mighty Mix salad mix (4 oz packages, Best By 1/23) due to potential contamination with small glass particles. No injuries have been reported; consumers should discard the product.
Maquet Cardiovascular is recalling Vasoshield Syringe Packs (Model VH-5001) because ink on the syringe logo may chip, creating a risk of foreign body complications and embolic events. The recall affects 530 units in the United States and 215 units outside the United States.
SIREtizer Hand Sanitizer is recalled for containing acetal and acetaldehyde above allowable limits and manufacturing defects, including one superpotent lot.
Siemens Luminos X-ray imaging systems may have a footrest that detaches from the patient table during use. The manufacturer is recalling 886 units distributed worldwide.
Superior Fresh Organic Spring Mix Family Pack is being recalled due to potential glass particle contamination. The recall affects 1,516 cases distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.
Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance defects: dull trocars, broken tips, lack of flexibility, and radiopacity issues. The 8,563 affected units were distributed worldwide.
Amerisource Health Services is recalling Rifampin Capsules USP 300 mg nationwide due to failed impurities and degradation specifications. Affected patients should contact their healthcare provider before using remaining inventory.
Cardinal Health is recalling Jackson-Pratt Channel Drains due to multiple reported performance defects including dull trocars, lack of flexibility, missing radiopacity, and broken tips. These issues may compromise insertion and drain function.
Akorn is recalling Ketorolac Tromethamine Ophthalmic Solution nationwide due to manufacturing practice deviations. The voluntary recall affects multiple lot numbers of the 0.5% formulation.
Klosterman Baking Company is recalling potato flour buns sold in Indiana, Ohio, and Tennessee due to products being held under insanitary conditions that could pose health risks.
Cardinal Health is recalling 750 units of Jackson-Pratt Channel Drains (10 mm) due to multiple performance issues including broken drain tips, lack of radiopacity, dull trocars, and reduced flexibility that could affect surgical outcomes.
Akorn Inc. voluntarily recalls 36,025 tubes of AK-POLY-BAC Bacitracin/Polymixin B eye ointment nationwide due to manufacturing process deviations affecting product quality and sterility.
Klosterman Baking Company is recalling onion buns and bread distributed in Indiana, Ohio, and Tennessee for products held under insanitary conditions. Consumers should discard affected items.
Cardinal Health recalls Jackson-Pratt Channel Drains due to reported defects including non-visibility on imaging, dull insertion trocars, reduced flexibility, and broken drain tips.
Superior Fresh is recalling Spring Mix lettuce products that may contain small glass particles. The affected packages were distributed in Indiana, Pennsylvania, Virginia, and Wisconsin.
Klosterman Baking Company is recalling 109,343 units of whole grain breads and baked goods sold in Indiana, Ohio, and Tennessee that were held under insanitary conditions. Products were delivered between December 12-16, 2022.
Klosterman Baking Company is recalling raisin breads and bagels that were held under insanitary conditions. About 109,343 units were distributed to Indiana, Ohio, and Tennessee.
Cardinal Health Jackson-Pratt Channel Drains are recalled for performance defects including dull trocars, broken tips, lack of flexibility, and lack of radiopacity. 220 units are affected.
Klosterman Baking Company is recalling French bread products (16 oz. loaves, SKUs 8510, 8550, 8551) distributed in Indiana, Ohio, and Tennessee because they were held under insanitary conditions.
Klosterman Baking Company is recalling 109,343 pretzel buns due to insanitary storage conditions. Products distributed to Indiana, Ohio, and Tennessee have expiration dates of December 21, 2022 or earlier.
Bolton Medical has recalled 640 units of RELAY PRO thoracic stent-graft systems worldwide because the products may be shorter than their packaging indicates.
Cardinal Health is recalling 2,277 Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. These defects may affect the drain's function and clinical performance.
Autocar is recalling 2021-2023 Xpeditor natural gas vehicles due to a software error in the instrument cluster fuel gauge. The inaccurate fuel gauge may cause the vehicle to unexpectedly run out of fuel and stall, increasing crash risk.