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.
Minimum severity
B.C. Williams Bakery Service is recalling Swiss Chocolate Cake Mix for containing undeclared milk allergen. Consumers with milk allergies should not consume this product.
JUICE from the Raw cashew coffee milk was under-processed and may contain pathogenic bacteria. The FDA issued a Class I recall; consumers should not use the product.
Boston Scientific is recalling 588 units of HOT AXIOS biliary stents worldwide due to reports of deployment and expansion failures that may require additional endoscopic or surgical intervention.
Outside The Breadbox bread crumbs are being recalled due to undeclared egg and milk allergens. The recall affects 4,497 units distributed across eight states.
Tai Phat Wholesalers, LLC is recalling Sofit Seedless Red Dates due to undeclared sulfites, an allergen. The 12 oz packages were distributed to Florida, Georgia, Iowa, and North Carolina.
Tradin Organics USA, LLC is recalling Organic Chia Seed Black from Paraguay due to potential Salmonella contamination. Product was distributed in California, Colorado, New York, and Canada.
Rheumacare capsules (30-count bottles) are being recalled due to lead contamination discovered during manufacturing. The affected product was distributed to one customer in New York and should not be used.
Everpress Juice is recalling JUICE from the Raw DETOX GREENS due to under-processing that may allow pathogenic bacteria to be present. The affected product was distributed across 23 states.
Boston Scientific is recalling the AXIOS Stent and Electrocautery-Enhanced Delivery System (20mm x 10mm) due to reports of stent deployment and expansion failures that may require additional surgical or endoscopic intervention.
Everpress Juice is recalling JUICE from the Raw, a cashew milk product, due to potential pathogenic bacteria from under-processing. The product was distributed across multiple U.S. states.
FDA Class I recall of AXIOS Stents due to reported deployment and expansion failures. Affected patients may require device exchange or additional surgical intervention to remove the stent and close the puncture site.
Boston Scientific is recalling 266 units of the HOT AXIOS Stent due to deployment and expansion issues that may require additional surgical intervention to remove the stent and close the puncture site.
Boston Scientific recalls HOT AXIOS 8mm stent delivery system for deployment and expansion failures. The devices may require surgical intervention to remove the stent and close puncture sites.
Boston Scientific is recalling AXIOS stents due to reported deployment and expansion issues. The devices may fail to expand properly during procedures, potentially requiring additional surgical intervention.
Everpress Juice is recalling JUICE from the Raw pineapple mint due to under-processing that may allow pathogenic bacteria to survive. The product was distributed across multiple states.
Everpress Juice is recalling its JUICE from the Raw sweet greens product due to potential pathogenic bacterial contamination. The product was distributed to 22 states.
B.C. Williams Bakery Service, Inc is recalling its spice cake mix in 50 lb. bags due to undeclared milk allergen. The product was distributed nationwide under Batch 221.
B.C. Williams Bakery Service is recalling Bread and Roll Mix sold nationwide due to undeclared milk allergen. Consumers with milk allergies could have serious allergic reactions if they consume this product.
Venzu Traders LLC is recalling cinnamon powder (3.5 oz packs) due to potential contamination with the heavy metal lead. The product was distributed in California, Nevada, and Washington.
Diva Fam Inc is recalling Sea Moss Gel Superfood (16 FL OZ) due to potential Clostridium botulinum contamination. The affected products were distributed nationwide through retail and online sales.
Focalyx Fusion prostate imaging devices may not work properly on Windows 10, risking patient harm during biopsy or treatment delays. The manufacturer recommends stopping use until Windows 11 compatibility is verified.
VANTIVE US HEALTHCARE LLC recalls PRISMAFLEX ST100 dialyzer sets nationwide due to potential dislodgement of the deaeration chamber from the control unit.
Olympus is recalling approximately 11,779 Single Use 3-Lumen Sphincterotome V surgical instruments distributed in the US. Some devices may not have undergone proper thermoforming, which could cause them to deform and lose performance during use.
Vivoo Protein Test strips were distributed without FDA clearance. The unapproved devices may produce false or inaccurate diagnostic results, potentially leading to inappropriate medical treatment.
Beckman Coulter is recalling specific lots of COULTER DxH Diluent due to elevated background counts in platelet Daily Checks when used with UniCel DxH analyzers. This can affect test result accuracy.