FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container
- Announced by FDA
- August 25, 2026
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Drug Recall 2026 record Source: FDA
Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 16, 2026
Drug Recall 2026 record Source: FDA
traZODone Hydrochloride Tablets, USP, 50 mg, Rx only, 100 Tablets, Manufactured in Croatia By: Pliva Hrvatska d.o.o, Zagreb, Croatia, Manufactured For: Teva Pharmaceuticals, Parsippany, NJ 07054, NDC 50111-560-01
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Ramipril Capsules USP, 10 mg, packaged in a) 100 Capsules (NDC 76282-673-01) and b) 500 Capsules (NDC 76282-673-05) bottles, Rx only, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33432, Manufactured by: West-Ward Columbus Inc., Columbus, OH 43228.
- Recall initiated
- August 24, 2026
- Reported by FDA
- September 2, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Thyroid Tablets, USP 30 mg
- Announced by FDA
- August 24, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Veggie Chips Broccoli Florets & Cauliflower
- Announced by FDA
- August 24, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Chocolate Dipped Vanilla Cake Donuts
- Announced by FDA
- August 24, 2026
Food Recall 2026 record Source: FDA
International Sprout Holdings, Inc
- Recall initiated
- August 23, 2026
- Reported by FDA
- September 16, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Everything Sprouts, LLC
- Recall initiated
- August 22, 2026
- Reported by FDA
- September 23, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Alfalfa Sprouts
- Announced by FDA
- August 22, 2026
Terminated
Drug Recall 2026 record Source: FDA
Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg, 100 Tablets, Rx only, Distributed by: Vitruvias Therapeutics, Auburn, AL 36830, Product of USA, NDC 69680-166-00.
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Prasugrel HCI, Tablets, USP, 10mg, 30-count bottle, Rx only, Marketed by: GSMS, Incorporated, Camarillo, CA 93012, USA, NDC: 51407-445-30.
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Broadway Joe's Pain Cream, 3000 gm CBD, (Histamine Dihydrochloride 0.025%) (CDB Isolate 3000mg, HempSeed Oil 2000mg),4 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-6; UPC 8 50041 64004 4
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Broadway Joe's Pain Cream, (Histamine Dihydrochloride 0.025%), 1500mg CBD Isolate, 1000mg Hempseed oil, 2 oz-jar, Produced for Broadway Joe's, Franklin, TN, 37067, NDC 83088-8120-5, UPC 8 50041 64003 7
- Recall initiated
- August 21, 2026
- Reported by FDA
- September 9, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Fromm wet canned dog food
- Announced by FDA
- August 21, 2026
Drug Recall 2026 record Source: FDA
AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5%, Lubricant Eye Drops, Sterile, 0.5 FL OZ (15 mL) EACH, 1.0 FL OZ (30 mL) TOTAL, 2 count Twin Pack, Distributed by: AVKARE, Pulaski, TN, 38478, NDC 50268-068-02 (carton)
- Recall initiated
- August 20, 2026
- Reported by FDA
- September 30, 2026
Drug Recall 2026 record Source: FDA
Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05
- Recall initiated
- August 20, 2026
- Reported by FDA
- September 30, 2026
Data last updated:
Investigations and recalls may be ongoing; status, case counts, and guidance are updated by the source agency as events continue. Read the full medical disclaimer.
