FDA Recall United States Ongoing Historical recordClass I
JFE FRANCHISING INC
- Product
- Diced Pepper Tri-Blend - 8 oz 639123880024 Diced Pepper…
- Reason
- Listeria monocytogenes
- Published
- September 11, 2024
- Distribution
- KY MI OH WV
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 Ongoing Historical recordClass I
JFE FRANCHISING INC
- Product
- Pico de Gallo Classic Hot - 14 oz 639123880116 Pico de G…
- Reason
- Listeria monocytogenes
- Published
- September 11, 2024
- Distribution
- KY MI OH WV
FDA Recall United States Ongoing Historical recordClass I
JFE FRANCHISING INC
- Product
- Salsa Medium - 16 oz Salsa Mild - 16 oz Plastic Clam-Shell…
- Reason
- Listeria monocytogenes
- Published
- September 11, 2024
- Distribution
- KY MI OH WV
FDA Recall United States Ongoing Historical recordClass I
JFE FRANCHISING INC
- Product
- Chopped Cilantro with White Onion - 5oz Plastic Clam-Shell C…
- Reason
- Listeria monocytogenes
- Published
- September 11, 2024
- Distribution
- KY MI OH WV
FDA Recall United States Ongoing Historical recordClass I
JFE FRANCHISING INC
- Product
- Butternut Squash Cubes - 12oz Plastic Clam-Shell Container
- Reason
- Listeria monocytogenes
- Published
- September 11, 2024
- Distribution
- KY MI OH WV
FDA Recall Terminated Historical recordClass II
Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA, NDC 68180-405-01
- Reason
- Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
IBU Ibuprofen Tablets, USP, 400 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a) NDC 55111-682-01 - 100 Tablets per bottle, b) NDC 55111-682-05 - 500 Tablets per bottle.
- Reason
- Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
IBU Ibuprofen Tablets, USP, 600 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-683-01 - 100 Tablets per bottle, b)NDC 5511-683-05 - 500 Tablets per bottle.
- Reason
- Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
IBU Ibuprofen Tablets, USP, 800 mg, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, a)NDC 55111-684-01 - 100 Tablets per bottle, b)NDC 55111-684-05 - 500 Tablets per bottle.
- Reason
- Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b) 90-count bottle (NDC 68462-325-90), Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Plot No. 2 Phase-2, Pharma Zone, SEZ, Pithampur, Dist-Dhar, Madya Pradesh - 454775, India Mfg Llc. No: 25/9/2010, Manufactured for Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430.
- Reason
- Failed Dissolution Specifications: below specification results
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
PARADISE DISTRIBUTORS, LLC
- Product
- Yummy brand Swirly Ices Assorted Flavors Net Wt. 2.3 ounces…
- Reason
- Undeclared milk.
- Published
- September 4, 2024
- Distribution
- Retail supermarkets in CA, NY, IL, FL, M…
FDA Recall United States Terminated Historical recordClass I
PARADISE DISTRIBUTORS, LLC
- Product
- Yummy brand Swirly Ices Churning Cherry flavor Net Wt. 2.3 o…
- Reason
- Undeclared milk.
- Published
- September 4, 2024
- Distribution
- Retail supermarkets in CA, NY, IL, FL, M…
FDA Recall United States Terminated Historical recordClass I
PARADISE DISTRIBUTORS, LLC
- Product
- Yummy brand Swirly Ices Fruity Melon flavor Net Wt. 2.3 ounc…
- Reason
- Undeclared milk.
- Published
- September 4, 2024
- Distribution
- Retail supermarkets in CA, NY, IL, FL, M…
FDA Recall United States Terminated Historical recordClass I
PARADISE DISTRIBUTORS, LLC
- Product
- Yummy brand Swirly Ices Berry Blast flavor Net Wt. 2.3 ounce…
- Reason
- Undeclared milk.
- Published
- September 4, 2024
- Distribution
- Retail supermarkets in CA, NY, IL, FL, M…
FDA Recall United States Terminated Historical recordClass I
PARADISE DISTRIBUTORS, LLC
- Product
- Yummy brand Swirly Ices Tropical Tornado flavor Net Wt. 2.3…
- Reason
- Undeclared milk.
- Published
- September 4, 2024
- Distribution
- Retail supermarkets in CA, NY, IL, FL, M…
FDA Recall United States Terminated Historical recordClass II
Alb-USA Enterprises Inc
- Product
- ALB Flavor brand CINNAMON Powder; 100 g; ALB-USA Enterprises…
- Reason
- Product contains elevated levels of lead (3.294ppm)
- Published
- September 4, 2024
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
NOW Foods
- Product
- NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag UP…
- Reason
- High mold, yeast, and total viable count
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Colonna Brothers Inc.
- Product
- Ground cinnamon. Supreme Tradition brand ground cinnamon p…
- Reason
- Elevated lead levels in cinnamon
- Published
- September 4, 2024
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
PBM Nutritionals, LLC
- Product
- CVS Health brand and HEB Baby brand Premium Infant Formula w…
- Reason
- Product contains levels of Vitamin D above the maximum level permitted.
- Published
- September 4, 2024
- Distribution
- Multiple states
FDA Recall Ongoing Historical recordClass II
Timolol Maleate Ophthalmic Solution USP, 0.5%, packaged in: a) 5mL bottle (NDC 64980-514-05), and b) 10mL bottle (NDC 64980-514-01), Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey
- Reason
- Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
- Published
- August 28, 2024
- Distribution
- Nationwide
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.
