FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container
- Announced by FDA
- September 3, 2026
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FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Organic Triple Berry Blend
- Announced by FDA
- September 3, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial
- Announced by FDA
- September 3, 2026
Drug Recall 2026 record Source: FDA
Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL) bottles (NDC 0536-1351-42), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152.
- Recall initiated
- September 1, 2026
- Reported by FDA
- October 7, 2026
Drug Recall 2026 record Source: FDA
Benzoyl Peroxide Wash, USP, 5%, 5 FL OZ (148 mL), Distributed by: Rugby Laboratories, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1259-63
- Recall initiated
- September 1, 2026
- Reported by FDA
- October 7, 2026
Drug Recall 2026 record Source: FDA
Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for: TerSera therapeutics LLC, Deerfield, IL 60015, BY: AstraZeneca UK Limited, Macclesfield, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36.
- Recall initiated
- August 31, 2026
- Reported by FDA
- October 7, 2026
Drug Recall 2026 record Source: FDA
Lidocaine Ointment USP, 5%, Speermint Flavor, 50 g Jar, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, L6T1C, Canada, Dist By: Taro Pharmaceuticals U.S.A. Inc. Hawthorne NY 70532 NDC: 51672-3008-5
- Recall initiated
- August 31, 2026
- Reported by FDA
- September 23, 2026
Drug Recall 2026 record Source: FDA
Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.
- Recall initiated
- August 31, 2026
- Reported by FDA
- September 9, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Lipofit Extreme 2.0 Fat Burner Dietary Supplement
- Announced by FDA
- August 31, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml
- Announced by FDA
- August 31, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.
- Announced by FDA
- August 31, 2026
Food Recall 2026 record Source: FDA
LMSI, LLC
- Recall initiated
- August 29, 2026
- Reported by FDA
- October 7, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Mangoes
- Announced by FDA
- August 29, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Robust Radish Mix, 5oz Cups
- Announced by FDA
- August 29, 2026
Drug Recall 2026 record Source: FDA
Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382213, India; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1685-1
- Recall initiated
- August 28, 2026
- Reported by FDA
- September 30, 2026
Food Recall 2026 record Source: FDA
Tiffany Food Corp
- Recall initiated
- August 28, 2026
- Reported by FDA
- September 23, 2026
Food Recall 2026 record Source: FDA
Frutas y Hortalizas del Sur S.A.
- Recall initiated
- August 28, 2026
- Reported by FDA
- September 23, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Chicken Recipe
- Announced by FDA
- August 28, 2026
Drug Recall 2026 record Source: FDA
Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ, 08540; Manufactured by: Macleods Pharmaceuticals, Ltd, Baddi, Himachal Pradesh, INDIA, NDC 33342-068-07.
- Recall initiated
- August 27, 2026
- Reported by FDA
- September 30, 2026
Food Recall 2026 record Source: FDA
FOODS ALIVE INC.
- Recall initiated
- August 26, 2026
- Reported by FDA
- September 23, 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.
