FDA Recall
🇺🇸 United States
TerminatedTerminated: September 30, 2025Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Grilling Camembert with Tapenade & Roasted Tomatoes…
- Reason
- Products may be contaminated with Listeria monocytogenes
- Published
- September 17, 2025
- Distribution
- NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 30, 2025Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Assorted Cheese Flight - Varies (sold by the lb) - B…
- Reason
- Products may be contaminated with Listeria monocytogenes
- Published
- September 17, 2025
- Distribution
- NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: September 30, 2025Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round…
- Reason
- Products may be contaminated with Listeria monocytogenes
- Published
- September 17, 2025
- Distribution
- NY, PA, MA, NJ, MD, VA, NC, DE, CT and D…
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FDA Recall
OngoingHistorical recordClass I
0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7800-09
by B BRAUN MEDICAL INC
- Reason
- Presence of Particulate Matter.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
Lactated Ringers's Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7750-07
by B BRAUN MEDICAL INC
- Reason
- Presence of Particulate Matter
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100-count bottles Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1062-1.
by Amneal Pharmaceuticals, LLC
- Reason
- Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100-count bottle, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1060-1.
by Amneal Pharmaceuticals, LLC
- Reason
- Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA; Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1058-1.
by Amneal Pharmaceuticals, LLC
- Reason
- Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottles, Rx Only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Oral Solid Dosage Unit, Ahmedabad 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 69238-1056-1.
by Amneal Pharmaceuticals, LLC
- Reason
- Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg, Double Strength, Rx Only, Packaged as a) 100-count bottle, NDC 65162-272-10; b) 500-count bottle, NDC 65162-272-50; Manufactured by: Amneal Pharmaceuticals, Pvt. Ltd, Oral Solid Dosage Unit, Ahmedabad, 382213, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807.
by Amneal Pharmaceuticals, LLC
- Reason
- Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore Commercial LLC, 181 Washington St, Conshohocken, PA, 19428, Product of Denmark NDC 80446-0401-01 Lot #: 3D009AA09, 3D009AA10, 3D009AA25, Exp Date: 31 MAR 2026 NDC 80446-0401-99 (Non-Commercial FG) Lot #: 3D009AA02, Exp Date 31 MAR 2026
by IMMUNOCORE, LLC
- Reason
- Subpotent Drug
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08
by DermaRite Industries, LLC
- Reason
- Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34
by DermaRite Industries, LLC
- Reason
- Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08
by DermaRite Industries, LLC
- Reason
- Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass I
DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E (Chloroxylenol 0.2%), packaged in a) 800 ml (27 fl. oz.) bag-n-box (NDC 61924-092-27) and b) 1000ml (34 fl. oz.) bag-n-box (NDC 61924-092-34) , DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
by DermaRite Industries, LLC
- Reason
- Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Semaglutide, 2.5 mg/mL injection, 4 mL, Boothwyn Pharmacy
by Boothwyn Pharmacy LLC
- Reason
- Subpotent Drug
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Semaglutide, 2.5 mg/mL injection, 0.8 mL, Boothwyn Pharmacy
by Boothwyn Pharmacy LLC
- Reason
- Subpotent Drug
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass III
Fluorescein 2% Ophth, 3 ML, Boothwyn Pharmacy, 800-476-7496
by Boothwyn Pharmacy LLC
- Reason
- Subpotent Drug
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
OngoingHistorical recordClass II
Semaglutide, 2.5 mg/mL injection, 2 mL., Boothwyn Pharmacy
by Boothwyn Pharmacy LLC
- Reason
- Subpotent Drug
- Published
- September 10, 2025
- Distribution
- Nationwide
View recall →
FDA Recall
🇺🇸 United States
TerminatedTerminated: February 20, 2026Historical recordClass I
Taylor Farms Retail, Inc.
- Product
- Salad Kit labeled as follows: Taylor FARMS Honey Balsamic SA…
- Reason
- Undeclared allergens (sesame and soy).
- Published
- September 10, 2025
- Distribution
- U.S. Distribution: AR, AZ, CA, CO, FL, I…
View recall →
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions.
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