FDA Enforcement Records
Explore FDA enforcement records
Browse published US FDA drug-enforcement recall records. Filter by country, classification, status, or date.
Showing 426–450 of 5,012 active FDA enforcement records
- View firm →Class IIOngoingLIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz · Jan 21, 2026 · United States
- View firm →Class IIOngoingEXCEDRIN MIGRAINE 2'S- 25 CT · Jan 21, 2026 · United States
- View firm →Class IIOngoingDAYQUIL COLD & FLU, 32CT/2PK · Jan 21, 2026 · United States
- View firm →Class IIOngoingClaritin, 20 Count, UPC: 655708016305 · Jan 21, 2026 · United States
- View firm →Class IIOngoingBenadryl, 25'S 2PK Box, UPC 815556020316 · Jan 21, 2026 · United States
- View firm →Class IIOngoingAlka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932 · Jan 21, 2026 · United States
- View firm →Class IIOngoingAdvil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559 · Jan 21, 2026 · United States
- View firm →Class IIOngoingAQ 120 GFEW, Aquarion Preserved Cartridges (2) 3.7 Gallons each · Jan 21, 2026 · United States
- View firm →Class IIOngoingLevothyroxine Sodium Tablets, USP, Thyro-Tabs, 150mcg, 1000 Tablets, Rx only, Manufactured by: LLOYD, Inc., Shenandoah, IA, 51601 USA, Distributed by: Alvogen, Inc., Pine Brook, NJ 07058 USA, NDC: 47781-662-10. · Jan 21, 2026 · United States
- View firm →Class IIOngoingTESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical Technology, 132 South Central Avenue, Elmsford, NY 10523, NDC# 57377-100-01 · Jan 21, 2026 · United States
- View firm →Class IIIOngoingClindamycin Phosphate USP, 1% (10 mg/mL), Topical Solution, 60 mL per applicator bottle, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel; Dist. by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC# 51672-4081-4 · Jan 21, 2026 · United States
- View firm →Class IIIOngoingFluocinolone Acetonide Solution Topical Solution USP, 0.01%, 60-mL bottles, Rx only, Dist. by: Taro Pharmaceuticals Inc., Hawthorn, NY 10532. NDC 51672-1365-4 · Jan 21, 2026 · United States
- View firm →Class IIOngoingRosuvastatin Tablets, USP, 10 mg, Rx Only, 50 Tablets (5 x 10) Unit Dose per carton, Manufactured for: AvKARE, Pulaski, TN 38478. NDC: 50268-709-15 · Jan 14, 2026 · United States
- View firm →Class IOngoingClearLife Allergy Nasal Spray, Extra Strength, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4006-9, UPC 787647101887 · Jan 14, 2026 · United States
- View firm →Class IOngoingReBoost Nasal Spray, 0.68 fl. oz. (20 mL) bottles, Distributed by: MediNatura, 10421 Research Rd., SE, Albuquerque, NM 87123, NDC 62795-4005-9, UPC 787647101863 · Jan 14, 2026 · United States
- View firm →Class IIOngoingOxycodone and Acetaminophen CII Tablets USP, 7.5 mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0522-01. Case label: SpecGx LLC, NDC 0406052201, Exp. 2027/03, Lot: 0522J23493 · Jan 14, 2026 · United States
- View firm →Class IIOngoingOxycodone and Acetaminophen CII Tablets USP, 10mg/325 mg, 100 tablets, Rx only, SpecGx LLC, Webster Groves, MO 63119, NDC 0406-0523-01. · Jan 14, 2026 · United States
- View firm →Class IIOngoingORL Kids Natural Toothpaste, Bubblegum Flavor, 4 oz (120ml), ORL Labs, LLC, Scottsdale, Arizona USA · Jan 14, 2026 · United States
- View firm →Class IIOngoingORL Kids Mouthwash, Bubblegum Flavor, 16.9 oz. (500ml) per bottle, ORL Labs, LLC, Scottsdale, Arizona USA · Jan 14, 2026 · United States
- View firm →Class IIOngoingTri-Moxi+¿ (Triamcinolone 9mg/0.6mL, Moxifloxacin 0.6 mg/ 0.6 mL) Single-Use Intraocular Injection, Imprimis NJOF, LLC., 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852. NDC 71384-746-06. · Jan 14, 2026 · United States
Only the latest five years of published US FDA drug-enforcement recall records are indexed. The displayed entity is an FDA-recorded recalling firm; country, city, and state are source attributes, not proof of manufacturer, parent company, ownership, legal entity, safety, compliance, or approval.