Agency
The FDA regulates food, drugs, biologics, medical devices, and tobacco. We aggregate Class I, II, and III enforcement actions across its three recall streams.
The FDA is the single biggest source of US product recalls by volume. Its enforcement workload splits into three streams — Foods (everything from infant formula to leafy greens to nutritional supplements), Drugs (prescription medicines, over-the-counter products, and active pharmaceutical ingredients), and Medical Devices (everything from implants to home blood-pressure monitors). The Recall Desk ingests all three from the openFDA enforcement endpoint every six hours.
FDA classifies every recall as Class I, II, or III. Class I means there is a reasonable probability that using the product will cause serious health consequences or death — these are the recalls you should treat as urgent. Class II means the product may cause temporary or medically reversible harm. Class III means the product is unlikely to cause adverse health consequences but still violates FDA rules. We map these classifications into our 1–5 severity score using the rubric on the methodology page.
Medical-device recalls are the highest-volume stream by far — software-update letters, calibration corrections, and IFU updates all show up in enforcement reports alongside genuine hazard recalls. We try to surface the severe ones first, but when in doubt, click through to the FDA notice itself for the clinical detail.
Albertsons store-made Parmesan Crusted Tilapia is being recalled because the contains statement does not declare tilapia. 15 units are affected.
Albertsons store-made Pop Dots Coco & Hazelnut, 6 count, is being recalled because the contains statement does not declare hazelnut. 25 units are affected.
Albertsons store-made Ready Meals Baked Pollock 4 count is being recalled because the contains statement does not declare pollock. Five units are affected.
Xyvona levorphanol tartrate tablets, 2 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Albertsons store-made Shrimp P&D Old Bay Seasoned is being recalled because the contains statement does not declare shrimp. Five units are affected.
Albertsons store-made Smoked Salmon & Feta Pasta Salad is being recalled because the contains statement does not declare salmon. 34 units are affected.
Albertsons store-made Shrimp Kabob 16-20 CT with Jamaican Jerk Marinade is being recalled because the contains statement does not declare shrimp. Five units are affected.
Albertsons store-made Meal Salmon Cajun is being recalled because the contains statement does not declare salmon. 40 units are affected.
Albertsons store-made Salmon Pesto with Asparagus is being recalled because the contains statement does not declare salmon. 149 units are affected.
Albertsons store-made Tempura Shrimp with Thai Sweet Chili Sauce is being recalled because the contains statement does not declare shrimp. 14 units are affected.
Albertsons store-made Shrimp Kabob 16-20 count with Kung Pao Marinade is being recalled because the contains statement does not declare shrimp.
Xyvona levorphanol tartrate tablets, 3 mg, are being recalled following FDA's denial of marketing the product under the proprietary name Xyvona.
Albertsons store-made Southwest Shrimp Bowls are being recalled because the contains statement does not declare shrimp. 23 units in total are affected.
Albertsons store-made almond croissants, sold under three UPCs, are being recalled because the contains statement does not declare almond. 104 units in total are affected.
Medline Industries, LP is recalling Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline Industries, LP is recalling specific Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection due to microbiology testing data integrity concerns and efficacy complaints.
Medline spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 30,120 kits are affected.
Parmesan & Herb Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.
A bulk banana smoothie base is being recalled because the firm received and used a potentially Salmonella-contaminated ingredient to manufacture various products. 4,980 pounds are affected.
Wawa Diet Lemonade in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 374 units are affected.
Medline spinal trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled over microbiology data integrity and efficacy complaints.
Wawa Fruit Punch in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 1,694 units are affected.
Wawa Beverage Company is recalling Wawa Iced Tea Lemon 16 oz Pint plastic bottles because they contain undeclared milk.
Medline spinal anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 200,702 kits are affected.
Medline pain trays and Whitacre spinal block trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 28,106 kits are affected.