FDA Recall United States Ongoing Historical recordClass II
Nature's Eudos Distributors LLC
- Product
- Eudos Bronquilan
- Reason
- Undeclared colors (FD&C Yellow #5, FD&C Blue #1, and FD&C Red #40)
- Published
- June 11, 2025
- Distribution
- NY and NJ
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,062
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,786
Class I recallsReasonable probability of serious health consequences24,313
Class II recallsTemporary or medically reversible health consequences2,876
Class III recallsNot likely to cause adverse health consequencesQuick insights
A snapshot of the most notable patterns across all recorded FDA and USDA recalls.
Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
53 recalls
Most common hazardLack of Assurance of Sterility
2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/evergreen-fresh-sprouts-llc-recalls-broccoli-sprouts-because-possible-health-riskPublished September 10, 2026
Download matching recalls as CSV
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A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,527 recalls have been announced year to date.
- Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
- The highest complete period was Jun 2026 (297).
- Sep 2026 is incomplete and not included in the figures above.
- Complete data
- Incomplete
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
FDA Recall United States Terminated Historical 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…
FDA Recall United States Terminated Historical 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…
FDA Recall Ongoing Historical recordClass I
ENDURANCE BOOST WITH HORNY GOAT WEED, 500mg, 20 capsules per carton, VEPEMVA Nutrition Supplement....rgy and Endurance, UPC X004BB9Z8N
- 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
FDA Recall Ongoing Historical 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
- Reason
- OOS results reported for the Dissolution (by UV) test.
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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.
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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.
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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.
- Reason
- CGMP Deviations; presence 'N-Nitroso Carvedilol I' Impurity above the recommended acceptable intake limit
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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
- Reason
- Failed Impurities/Degradation Specifications
- Published
- June 4, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical 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…
FDA Recall Ongoing Historical 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.
- Reason
- cGMP deviations
- Published
- May 28, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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.
- Reason
- cGMP deviations
- Published
- May 28, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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, .
- Reason
- Defective delivery system
- Published
- May 28, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical 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
- 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
FDA Recall Ongoing Historical 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
- 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
FDA Recall Ongoing Historical recordClass II
BD ChloraPrep Clear, 2% x/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA), Patient Preoperative Skin Preparation, Sterile Solution, Applicator is sterile if package is intact, Flammable, External Use Only, 1 mL Applicator per pouch, 60 Applicators per inner carton, CareFusion 213, LLC, El Paso, TX 79912, subsidiary of Becton, Dickinson and Co., Made in the USA, Catalog Number 930480, NDC 54365-400-31.
- Reason
- Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.
- Published
- May 28, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
BBF Massachusetts LLC
- Product
- Zeke's Daddy's Granola; INGREDIENTS: Whole grain rolled oats…
- Reason
- Product contains undeclared almond and cashew.
- Published
- May 28, 2025
- Distribution
- NJ
FDA Recall United States Terminated Historical recordClass I
My Life Inc
- Product
- Lactoferrin as Apolactoferrin 60 vegetarian capsules, 300 mg…
- Reason
- Undeclared milk allergen
- Published
- May 28, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Advantage Health Matters Inc.
- Product
- Organic traditions brand JUMBO PUMPKIN SEEDS; 227 g; 8 oz; P…
- Reason
- Product may be contaminated with Salmonella
- Published
- May 28, 2025
- Distribution
- Multiple states
Data last updated:
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. Read the full medical disclaimer.
