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
Teleflex Medical is voluntarily recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube.
Maine Wild Blueberry Company is recalling 30-lb cases of frozen wild blueberries after internal sampling detected Listeria monocytogenes. The product was not distributed to consumers.
Cook Inc. is recalling 131 Advance Enforcer 35 Focal Force PTA Balloon Catheters because multiple complaints reported the balloons bursting below their rated pressure.
Bobbie Baby is recalling specific lots of Milk-Based Powder Companion Formula because the product does not provide adequate nutrition for some infants.
Mothers' Milk Bank at Austin is recalling 54 bottles of pasteurized donor human breast milk due to a positive microbiological culture for Bacillus cereus.
Heritage Pharmaceuticals is recalling Prochlorperazine Edisylate Injection because microbial growth was detected in a sublot. The affected vials are distributed nationwide.
Select Distributions LLC is recalling Aphrodisiac Platinum 40000 because FDA analysis found the product is tainted with sildenafil and was marketed without an approved NDA/ANDA.
Heritage Pharmaceuticals is recalling Amikacin Sulfate Injection vials because microbial growth was detected in a sub-lot. The affected product is distributed nationwide in the USA.
Icco Cheese Co Inc is recalling Gia Russa Whole Grain Italian Seasoned Bread Crumbs because the product contains undeclared walnuts and pecans.
Taylor Farms Illinois is recalling 51 pounds of Jarlsberg and bacon quiche because the label failed to list eggs, a known allergen.
Stiff Boy LLC is recalling The Beast because FDA analysis found undeclared sildenafil. The product was marketed without an approved NDA or ANDA.
House of Spices India, Inc. is recalling Laxmi Brand Dried Apricots because the product contains elevated levels of undeclared sulfites.
Great American Marketing Company is recalling Turkey and Swiss Sandwiches in Texas due to potential Listeria monocytogenes contamination.
Great American Marketing Company is recalling Ham and Cheddar Sandwiches in Texas due to potential Listeria monocytogenes contamination.
Mecox Bay Dairy is recalling Sunrise Raw Milk Cheese after New York State sampling detected Listeria monocytogenes. The product was distributed in New York and Chicago.
Great American Marketing Company is recalling Turkey Pepper Jack 6" Sub Sandwiches in Texas due to potential Listeria monocytogenes contamination.
Novartis is recalling Promacta (eltrombopag olamine) 12.5 mg oral suspension due to possible cross-contamination with peanut flour.
Great American Marketing Company is recalling Deli Cut Turkey Sandwiches in Texas due to potential Listeria monocytogenes contamination.
Life Rising Corporation is recalling 52 bottles of HoliCare Metabolism Cleansing tablets because they contain high levels of lead. The products were sold locally in the Chicago area and via mail order.
Great American Marketing Company is recalling Italian 6-inch sub sandwiches in Texas due to potential Listeria monocytogenes contamination.
Life Rising Corporation is recalling Holder-W Holder Warmer capsules due to high lead levels. The products were sold locally in the Chicago area and via mail order.
D.B.P. Distribution is recalling Titanium 4000 capsules because they contain undeclared sildenafil and tadalafil and were marketed without an approved NDA or ANDA.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Schiff Foods Products is recalling 50 lb. boxes of Jalapeno Powder because the product was found to contain Salmonella. The recall covers domestic and international distribution.