FDA Recall United States Terminated Historical recordClass I
Adm Milling
- Product
- King Arthur All Purpose Flour 25# bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
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/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026
Download matching recalls as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
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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 | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass I
Adm Milling
- Product
- Robin Hood All-purpose Flour in 5 lb bag UPC 051500180105
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
FDA Recall United States Terminated Historical recordClass I
Adm Milling
- Product
- King Arthur All-purpose Flour in 5 lb bag UPC 071012010509
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
FDA Recall United States Terminated Historical recordClass I
Adm Milling
- Product
- Bakers Corner All Purpose Flour in 5 lb. bags
- Reason
- E.coli O26
- Published
- February 19, 2020
- Distribution
- AR CT FL IL IN MA MD MI NJ NY…
FDA Recall United States Completed Historical recordClass II
Market America Inc
- Product
- bliss anti-stress formula Dietary Supplement, 60 Tablets; Ma…
- Reason
- Potentially undeclared Yohimbe 83 and complaints of adverse reactions: upset stomach, jittery, sweaty, lightheaded or dizzy.
- Published
- February 19, 2020
- Distribution
- Product was shipped to the following sta…
FDA Recall Terminated Historical recordClass III
Pioglitazone and Metformin Hydrochloride Tablets, USP 15 mg/500 mg, Rx Only, 60-count bottle, Manufactured for Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Himachal Pradesh, India, NDA 33342-176-09
- Reason
- Subpotent Drug: Out of specification assay result, below specification, for two lots of Pioglitazone And Metformin Hydrochloride Tablets.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Atorvastatin Calcium Tablets, USP, 10 mg*, 90-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009 USA; Manufactured By: Graviti Pharmaceuticals Pvt. Ltd., Telangana -502307, INDIA; NDC 70377-027-11.
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that one 20 mg Atorvastatin Calcium Tablet was present in a bottle labeled as and containing eight-nine Atorvastatin Calcium Tablets, USP 10 mg.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Desmopressin Acetate Tablets, 0.2 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2465-01
- Reason
- GMP Deviations: Product bottle may be absent of desiccant.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Desmopressin Acetate Tablets, 0.1 mg, 100-count bottle, Rx Only, Manufactured by: Actavis Laboratories, Inc. Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc. Parisppany, NJ 07054 USA, NDC 0591-2464-01
- Reason
- GMP Deviations: Product bottle may be absent of desiccant.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Clonidine Hydrochloride Tablets, USP 0.1mg, Rx Only, 100-count bottle, Manufactured by: Unichem Laboratories Ltd. Pilerne Ind. Estate, Pilerne Bardez, Goa 403 511 India. Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816. NDC 29300-135-01
- Reason
- Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container label.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Olmesartan Medoxomil Tablets 20 mg, Rx Only, 90 Tablets per Bottle, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013 INDIA, Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054, NDC 67877-446-90.
- Reason
- cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Minocycline Hydrochloride Extended-Release Tablets, USP, 105 mg*, 30-count bottle, Rx Only, Manufactured by: Alkem Laboratories Ltd., Mumbai - 400 013 India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054, NDC 67877-438-30.
- Reason
- Failed Dissolution Specifications: low out of specification results for dissolution testing.
- Published
- February 12, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles ( NDC 43063-844-14); b) 30-count bottles (NDC 43063-844-30); c) 60 -count bottles( NDC 43063-844-60); d) 90-count bottles (NDC 43063-844-90); e) 100-count bottles ( NDC 43063-844-01), Rx Only, Distributed by: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127
- Reason
- CGMP Deviations: Received notice from supplier of potential -Nitrosodimethylamine (NDMA) amounts above established levels.
- Published
- February 12, 2020
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Beepas LLC
- Product
- Beepa's Original Goulash Starter, 32 oz. (2 PTS) 946.35ml.…
- Reason
- Beepa's Goulash Starter contains undeclared milk.
- Published
- February 12, 2020
- Distribution
- IL and WI
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Fresh Grab Ham & Cheese on White Wedge Sandwich, 5 oz., UPC:…
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo Meat Lovers Sub, 7 oz., UPC: 612510093832
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo Italian Footlong Sandwich, 8 oz., UPC: 612510093535
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo Ham & Cheese on a Hawaiian Bun, 6 oz., UPC: 6125100935…
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Premo Bologna & Cheese Wedge Sandwich 5 oz., UPC: 6125100933…
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
FDA Recall United States Terminated Historical recordClass I
Lipari Foods Operating Company, LLC.
- Product
- Fresh Grab Ham & Cheddar with Chipotle Mayo, 6 oz., UPC: 61…
- Reason
- Products recalled due to potential contamination with Listeria monocytogenes
- Published
- February 12, 2020
- Distribution
- The products were distributed exclusivel…
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.
