Food Recall 2026 record Source: FDA
Wonton Specialists
- Recall initiated
- July 28, 2026
- Reported by FDA
- September 9, 2026
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Food Recall 2026 record Source: FDA
Wonton Specialists
- Recall initiated
- July 28, 2026
- Reported by FDA
- September 9, 2026
Food Recall 2026 record Source: FDA
Wonton Specialists
- Recall initiated
- July 28, 2026
- Reported by FDA
- September 9, 2026
Food Recall 2026 record Source: FDA
Wonton Specialists
- Recall initiated
- July 28, 2026
- Reported by FDA
- September 9, 2026
Drug Recall 2026 record Source: FDA
Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., Tarrytown, NY 10591; Marketed by: Regeneron Pharmaceuticals, Inc. (Tarrytown, NY 10591), NDC 61755-008-01
- Recall initiated
- July 28, 2026
- Reported by FDA
- August 26, 2026
Food Recall 2026 record Source: FDA
529 COMMERCE, LLC
- Recall initiated
- July 28, 2026
- Reported by FDA
- August 19, 2026
Food Recall 2026 record Source: FDA
FlavorsandColor.Com
- Recall initiated
- July 28, 2026
- Reported by FDA
- August 19, 2026
FDA Food Recall Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling, 11.6 oz (330 g), UPC 4056489125839
- Announced by FDA
- July 28, 2026
FDA Announcement - Pending Structured Confirmation 2026 record Source: FDA-ANNOUNCE
Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL
- Announced by FDA
- July 27, 2026
Drug Recall 2026 record Source: FDA
niCARdipine Hydrochloride Injection, USP, 25 mg/10mL (2.5 mg/mL), packaged in a) 10 mL Single Dose Vial (NDC 72572-470-01) and b) 10x10 mL Single Dose Vials (NDC 72572-470-10), Rx Only, Mfd for: Civica, Inc., Lehi, UT, Mfd by: American Regent, Inc., New Albany, OH 43054.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Tralement (trace elements injection 4*, USP), packaged in a) 1mL Single Dose vials (NDC 0517-9305-01) and b) 5x1mL Single Dose vials (NDC 0517-9305-25), Rx only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Papaverine HCl Injection, USP, 60 mg/2 mL (30 mg/mL), packaged in a) 2mL Single-Dose Vial (NDC 0517-4002-01), and b) 25x2mL Single-Dose Vials (NDC 0517-4002-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Multrys (Trace Elements Injection 4, USP), For intravenous infusion, packaged in a) 1 mL Single-Dose Vial (NDC 0517-9302-01), and b) 25x1 mL Single-Dose Vials (NDC 0517-9302-25) Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Selenious Acid Injection, USP 12 mcg/2 mL (6 mcg/2mL), For intravenous use, packaged in a) 2mL Single-Dose Vial (NDC 0517-6502-01), and b)10x2mL Single-Dose Vial (NDC 0517-6502-10), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
ACETYLCYSTEINE SOLUTION, USP, 20% (200 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7604-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC 0517-7604-25), Rx only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
ACETYLCYSTEINE SOLUTION, USP, 10% (100 mg/mL), packaged in a) 4 mL Vial NOT FOR INJECTION (NDC 0517-7504-01), and b) 25x4 mL Vials NOT FOR INJECTION (NDC 0517-7504-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Atropine Sulfate injection, USP, 1 mg/mL, For intravenous Use, Sterile, packaged in a) 1 mL Single-Dose Vial (NDC 0517-1001-01), and b) 25x1 mL Single-Dose Vial (NDC 0517-1001-25), Rx only, AMERICAN REGENT INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
AMINAOCAPROIC ACID INJECTION, USP, 250 mg/mL (5 g/20 mL), packaged in a) 20 mL MULTIPLE DOSE VIAL FOR IV INFUSION (NDC 0517-9120-01), and b) 25x20 mL MULTIPLE DOSE VIALS (NDC 0517-9120-25), Rx Only, American Regent, Inc., Shirley, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Cyanocobalamin injection USP, 10,000 mcg/10 mL (1,000 mcg/mL), For IM or SC Use Only, packaged in a) 10 mL Multi-Dose Vial (NDC 0517-0032-01) and b) 25x10 mL Multi-Dose Vials (NDC 0517-0032-25), Rx Only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 2026
Drug Recall 2026 record Source: FDA
Cyanocobalamin injection USP, 1,000 mcg/mL, For IM or SC Use Only, packaged in a) 1 mL Multi-Dose Vial (NDC 0517-0031-01), and b) 25x1 mL Multi-Dose Vials (NDC 0517-0031-25) Rx only, AMERICAN REGENT, INC., SHIRLEY, NY 11967.
- Recall initiated
- July 24, 2026
- Reported by FDA
- August 26, 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.
