FDA Recall
🇺🇸 United States
TerminatedTerminated: August 7, 2025Historical recordClass II
Pepsi Beverages Company
- Product
- Dr. Pepper, ZERO SUGAR, 12 FL OZ (355 mL) ALUMINUM CAN packa…
- Reason
- Product labeled to be Zero Sugar contains full sugar product.
- Published
- June 11, 2025
- Distribution
- Product was shipped to the following sta…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: July 21, 2025Historical recordClass I
pennrose farms LLC
- Product
- Cucumbers Pennrose Farms, Net Wt. 5lbs(2.26kg) Mesh bag, Dis…
- Reason
- Due to potential Salmonella Contamination
- Published
- June 11, 2025
- Distribution
- Product was shipped to FL, NJ, GA, IL, O…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 16, 2025Historical recordClass II
Publix Super Markets, Inc.
- Product
- Greenwise Pear Kiwi Spinach & Pea Baby Food Pouch. Net Wt 4…
- Reason
- Elevated levels of Lead, cadmium and arsenic
- Published
- June 11, 2025
- Distribution
- Multiple states
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FDA Recall
🇺🇸 United States
TerminatedTerminated: September 16, 2025Historical recordClass I
Bedner Growers, Inc.
- Product
- Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10…
- Reason
- Cucumbers may be potentially contaminated with Salmonella
- Published
- June 11, 2025
- Distribution
- Florida
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FDA Recall
🇺🇸 United States
TerminatedTerminated: June 17, 2025Historical recordClass III
GNC Holdings LLC
- Product
- GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet…
- Reason
- Undeclared Fish allergen (parvalbumin).
- Published
- June 11, 2025
- Distribution
- The adulterated product was distributed…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: March 18, 2026Historical recordClass III
Nordic Naturals, Inc.
- Product
- Nordic Naturals Zero Sugar Kids Multivitamin Supplement - Gu…
- Reason
- Product is mislabeled.
- Published
- June 11, 2025
- Distribution
- Domestic: AK, AZ, CA, CO, FL, GA, ID, IN…
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FDA Recall
🇺🇸 United States
TerminatedTerminated: November 7, 2025Historical recordClass II
Treehouse Foods
- Product
- Sysco Classic chocolate pudding, 7lb #10 metal can, UPC 0748…
- Reason
- Post process damage to containers, potential for microbial growth, swollen and or exploding containers
- Published
- June 11, 2025
- Distribution
- Arizona Arkansas California Florida Idah…
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FDA Recall
OngoingHistorical recordClass I
ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N
by EnShiShiXiangNiShangMaoYouXianGongSi
- Reason
- Marketed without approved NDA/ANDA: The product has been found to be tainted with Sildenafil and Propoxyphenylsildenafil (a sildenafil analogue).
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Theophylline (Anhydrous) Extended-Release Tablets, 600 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited. Colvale-Bardez, Goa - 403513, India. Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-356-01
by Glenmark Pharmaceuticals Inc., USA
- Reason
- OOS results reported for the Dissolution (by UV) test.
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Carvedilol Tablets USP 25 mg, 500 -Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC 68462-165-05.
by Glenmark Pharmaceuticals Inc., USA
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Carvedilol Tablets USP 12.5 mg, 500-Count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430. NDC: 68462-164-05
by Glenmark Pharmaceuticals Inc., USA
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Carvedilol Tablets USP 6.25 mg, a.)100-count bottle (NDC 68462-163-01), b.) 500-count bottle (NDC 68462-163-05) Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.
by Glenmark Pharmaceuticals Inc., USA
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Carvedilol Tablets USP 3.125mg Tablets a.)100-count bottle (NDC 68462-162-01), b.) 500-count bottle (NDC 68462-162-05), Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.
by Glenmark Pharmaceuticals Inc., USA
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Bromfenac Ophthalmic Solution 0.09%, 1.7 mL bottle, Rx only, Sterile, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, Manufactured by Alembic Pharmaceuticals Limitied, Gujarat, India, Made in India, NDC 62332-508-17
by Alembic Pharmaceuticals Limited
- Reason
- Failed Impurities/Degradation Specifications
- Published
- June 4, 2025
- Distribution
- Nationwide
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FDA Recall
🇺🇸 United States
TerminatedTerminated: February 11, 2026Historical recordClass I
HAWAIIAN HOST CANDIES OF LA INC
- Product
- Mauna Loa Dark Chocolate Covered Macadamias product is a sna…
- Reason
- Undeclared almond and cashew.
- Published
- June 4, 2025
- Distribution
- Distributed in AZ, CA, CO, FL, HI, IL, M…
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FDA Recall
OngoingHistorical recordClass II
Phentermine Hydrochloride Capsules, USP 30mg, 100-count bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-028-01.
by KVK Tech, Inc.
- Reason
- cGMP deviations
- Published
- May 28, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown, PA, 18940, Made in USA, NDC 10702-016-01.
by KVK Tech, Inc.
- Reason
- cGMP deviations
- Published
- May 28, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation, packaged in a) 120-inhalation canister (NDC 0310-9080-12) b) 28-inhalation canister (NDC 0310-9080-28), Rx only, Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850, By: AstraZeneca Dunkerque Production (AZDP), Dunkerque, France, Product of France, .
by AsttraZeneca Pharmaceuticals LP
- Reason
- Defective delivery system
- Published
- May 28, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 20 mg, 30-count single dose packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-848-94
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability.
- Published
- May 28, 2025
- Distribution
- Nationwide
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FDA Recall
OngoingHistorical recordClass II
Esomeprazole Magnesium for Delayed-Release Oral Suspension, 40 mg, 30-count Single-Dose Packets per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Ahmedabad, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-849-94
by Zydus Pharmaceuticals (USA) Inc
- Reason
- Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation product during Related Compounds testing during long term stability.
- Published
- May 28, 2025
- Distribution
- Nationwide
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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