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
Hillside Orchard Farms Jalapeno Cheese Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Peach Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Blueberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Blueberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Strawberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Cinnamon Pecan Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
ENDOTAK RELIANCE G/SG defibrillation leads with the 4-SITE connector are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils.
BMW is recalling certain 2026 X5, X5 Plug-in Hybrid, and X7 vehicles because the windshield may not be sealed properly, allowing water to enter electrical components and potentially causing headlight failure or fire.
Bayonet Luer-Lock injection needles, models 50-353-23 and 50-345-23, are recalled because affected product showed elevated cytotoxicity values, which may present a risk of intolerance or allergic reaction.
Biscuit Mix packed exclusively for Chick-fil-A, Inc. in 2.625 lb bags is recalled for undeclared eggs. The recall covers 150 cases of 12 bags.
Carvedilol Tablets USP, 12.5 mg, packaged by Major Pharmaceuticals, lot T05693, are recalled nationwide because N-Nitroso Carvedilol Impurity-1 exceeded the FDA-recommended 4.0 ppm limit. 26,628 cartons are affected.
Pentax Medical EPK-i8020c video processors are recalled after reports of darkened images, smoke-like steam and a hot endoscope light guide that may cause thermal injury to the patient's mucous membrane. 144 units are affected.
Estrone RIA kits, catalog number DSL8700, are recalled because certain lots may rarely give falsely high or falsely low patient results. 279 units are affected.
Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.
Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250123, are recalled because they are potentially contaminated with norovirus. 828 cartons are affected.
BZK Antiseptic Towelettes containing benzalkonium chloride 0.13%, sold 100 per carton for professional use, are recalled for lack of assurance of sterility. The recall covers 3.85 million cartons.
Burr Hole Cover Kits used with the Vercise Deep Brain Stimulation System are recalled because resistance closing the retaining clip may cause procedural delay or lead migration requiring further surgery. 24,583 units are affected.
Sri Sri Tattva Ojasvita Chocomalt, 7 oz / 200 g paper pouches, is recalled because it contains undeclared soy lecithin. 1,100 units are affected.
The ESG-410 Electrosurgical Generator is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 155 units are affected.
The ESG-410 Legacy Electrosurgical Generator, model WA91307C, is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 434 units are affected.
OtoLase Starter Kits, UPN AC-2003748, batches 32644549 and 32769567, are recalled because finished product labeled as sterile may not have been sterilized. 13 units are affected.
Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250112, are recalled because they are potentially contaminated with norovirus. 98 cartons are affected.
7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.
Raw Ramen Noodle HA #22W (4942) in 10 lb bulk cases, made by Kobayashi Noodle USA, is recalled because the label does not declare soy as the source of the lecithin ingredient. 2,800 cases are affected.
Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.