FDA Recall United States Terminated Historical recordClass I
ADM - CHICAGO
- Product
- Gold Medal Flour Product Code: 805046 Bulk flour
- Reason
- potential presence of E. coli. O26
- Published
- July 24, 2019
- Distribution
- Nationwide
Data Explorer
Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.
Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,137
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,799
Class I recallsReasonable probability of serious health consequences24,349
Class II recallsTemporary or medically reversible health consequences2,891
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/berlin-seeds-recalls-alfalfa-sprouting-seed-because-possible-health-riskPublished September 23, 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 | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,349 |
| Class I | 9,799 |
| Class III | 2,891 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass I
ADM - CHICAGO
- Product
- Miss Minneapolis Product Code: 803003 Bulk flour
- Reason
- potential presence of E. coli. O26
- Published
- July 24, 2019
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
ADM - CHICAGO
- Product
- Baker's Corner All Purpose Flour 5 lb. bag UPC code: 041…
- Reason
- potential presence of E. coli. O26
- Published
- July 24, 2019
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Perrigo Company PLC
- Product
- Parent's Choice Advantage Infant Formula Milk-Based Powder w…
- Reason
- Product may contain metal fragments.
- Published
- July 24, 2019
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Sprout's Farmers Market
- Product
- Sprouts Farmers Market Organic Cut Leaf Spinach, Net Wt 16 O…
- Reason
- Testing revealed the presence of Listeria monocytogenes in the frozen spinach
- Published
- July 24, 2019
- Distribution
- The product was shipped from the manufac…
FDA Recall United States Terminated Historical recordClass II
Sprout's Farmers Market
- Product
- Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb)…
- Reason
- Testing revealed the presence of Listeria monocytogenes in the frozen spinach
- Published
- July 24, 2019
- Distribution
- The product was shipped from the manufac…
FDA Recall United States Terminated Historical recordClass I
Frito-Lay, Inc.
- Product
- Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7…
- Reason
- Undeclared milk
- Published
- July 24, 2019
- Distribution
- Arkansas, Arizona, California, Colorado…
FDA Recall United States Terminated Historical recordClass III
Wilton Brands
- Product
- Wilton Chocolate decorator icing stiff consistency 16 oz…
- Reason
- Mold
- Published
- July 24, 2019
- Distribution
- AL AR AZ CA CO CT DE FL GA IA…
FDA Recall United States Terminated Historical recordClass II
Oregon Potato Company
- Product
- Frozen whole Red Raspberries; packed in a 12 oz. polyethylen…
- Reason
- Whole Red Raspberries are recalled due to potential contamination with Norovirus.
- Published
- July 24, 2019
- Distribution
- distributed in Arizona, California, Idah…
FDA Recall Terminated Historical recordClass II
Anastrozole Tablets, USP, 1 mg, a) 30-count (NDC 68001-155-04) and 1000-count (NDC 68001-155-08) bottles, Rx Only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories
- Reason
- GMP Deviations: Potential cross contamination due to cleaning procedure failure.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP. 50 mg. NDC# 0904-6390-61. Rx only. 100 count Unit Dose Cartons. Manufactured by Major Pharmaceuticals 17177 N. Laurel Park Drive Suite 233, Livonia, MI 48152.
- Reason
- CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium, 100 mg tablets, 90 count bottle, NDC 60429-318-90
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium, 50 mg tablets, 1000 count bottle, NDC 60429-317-10
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium, 50 mg tablets, 90 count bottle, NDC 60429-317-90
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium andHydrochlorothiazide Tablets 100 mg/25 mg 90 tablets, USP Rx Only, Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-052-10
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-051-10
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 90 Tablets, USP Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-050-10
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets 50 mg 1000 Tablets, USP Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-44
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Losartan Potassium Tablets, USP 50 mg 90 tablets Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals, Ltd. Baddi, Himachal Pradesh, INDIA NDC 33342-045-10
- Reason
- CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
- Published
- July 17, 2019
- 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.
