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
Albertsons store-made Platter Loaf Sliced, 20 count, is being recalled because the contains statement does not declare walnut. 20 units are affected.
Aligned Medical AMS16835 Fluids Kits are being recalled because they include Lidocaine Hydrochloride Injection, USP that was recalled by a supplier for quality issues.
Albertsons store-made Cake Cakerie Strawberry Shortcake Triangle is being recalled because the contains statement does not declare hazelnut. 71 units are affected.
Albertsons store-made Tray Charcuterie Elegant is being recalled because the contains statement does not declare pistachio. Eight units are affected.
Family Wellness Ultra Strength Antacid Tablets, calcium carbonate 1000 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Betaine Anhydrous 98% distributed by Creative Compounds is being recalled because of possible carbon steel foreign material of 1 to 2 mm. 2,055 kg are affected.
Philips Azurion 7B12/12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
The Andronico's Sweet Start Catering Tray Large, an Albertsons store-made item, is being recalled because the contains statement does not declare walnut. 14 units are affected.
Second Nature Keto Crunch Smart Mix is being recalled because the product may contain undeclared allergens, specifically cashews and pistachios, along with dried cherries.
Albertsons store-made seafood salad is being recalled because the contains statement does not declare crab. 114 units are affected.
Harris Teeter Ultra Strength Antacid, calcium carbonate 1000 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
The BD Pyxis MedStation ES medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
24/7 life by 7-Eleven Extra Strength Antacid Tablets, calcium carbonate 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
Hy-Vee Extra Strength Antacid, calcium carbonate 750 mg, is being recalled because of the presence of small metallic particles in the chewable tablets.
Sharpoint 2.2 mm angled double-bevel microsurgical knives are being recalled because 3.0 mm knives were labeled and packaged as 2.2 mm. 1,818 units affected.
Philips Azurion 3M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Denago EV is recalling 2024-2026 electric vehicles that may fail to emit pedestrian warning sounds, increasing the risk of crashes.
Albertsons store-made Ready Meals Salad Waldorf is being recalled because the contains statement does not declare walnut. 82 units are affected.
H.E.B Extra Strength Calcium Carbonate Antacid Tablets, 750 mg, are being recalled because of the presence of small metallic particles in the chewable tablets.
The BD Pyxis MedBank Tower medication cabinet is being recalled because the fingerprint scanner may overheat to a temperature capable of causing a first degree burn.
Albertsons store-made Dubai Chocolate Croissants, 2 count, are being recalled because the contains statement does not declare pistachio. 92 units are affected.
Albertsons store-made Kale Mango & Coconut Salad is being recalled because the contains statement does not declare cashew. 271 units in total are affected.
Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, are being recalled after failing dissolution specifications, with olmesartan medoxomil content below specification.
Philips Azurion 7M12 systems with the Roadmap Pro software key are being recalled because a pedal tap may cause a dark, clinically unusable image on the next fluoroscopy run.
Digital angiography and radiography systems are being recalled because contactors in the high voltage generator may weld together, leaving the power supply energized when the system is off.