FDA Recall United States Terminated Historical recordClass II
GARZA FOOD VENTURES
- Product
- Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8…
- Reason
- Potential to contain foreign material.
- Published
- June 3, 2020
- 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.
37,115
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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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 | 24,343 |
| 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 Terminated Historical recordClass III
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
- Reason
- Failed Impurities/Degradation Specifications: Out of Specification for impurity 6 and total degradants.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc., Lawrenceville, GA 30046, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY 11788, NDC 76282-405-05.
- Reason
- Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA. NDC: 67457-187-50
- Reason
- Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
- Reason
- Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
- Reason
- Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Pink Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA NDC 0573-0873-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA NDC 0573-0872-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA, NDC 0573-0871-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Middle East Bakery, Inc.
- Product
- Joseph's Gluten Free Original Wrap, 4 wraps, Net. Wt. 5.6 oz…
- Reason
- Gluten free wrap contains gluten
- Published
- May 20, 2020
- Distribution
- Multiple states
FDA Recall Terminated Historical recordClass II
Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed by: Baxter Healthcare Corporation Clintec Nutrition Division Deerfield, IL 60015 USA, NDC 54643-5647-0
- Reason
- Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
- Published
- May 13, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Glaxosmithkline Consumer Healthcare Holdings
- Product
- Benefiber Prebiotic Fiber Supplement, packaged in the follow…
- Reason
- Fiber prebiotic product potentially contaminated with small plastic pieces
- Published
- May 13, 2020
- Distribution
- Distributed to the following US states:…
FDA Recall United States Terminated Historical recordClass II
Glaxosmithkline Consumer Healthcare Holdings
- Product
- Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UP…
- Reason
- Fiber prebiotic product potentially contaminated with small plastic pieces
- Published
- May 13, 2020
- Distribution
- Distributed to the following US states:…
FDA Recall United States Terminated Historical recordClass I
Jason Pharmaceuticals, Inc. t/a Medifast
- Product
- Optavia, Old Fashioned Maple & Brown Sugar Oatmeal . 1.13 o…
- Reason
- The product contains undeclared milk.
- Published
- May 13, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Aldi Inc
- Product
- Simply Nature Organic Red Split Lentils, 16 oz bag, UPC 0414…
- Reason
- Product may contain undeclared wheat
- Published
- May 13, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Aldi Inc
- Product
- Simply Nature Organic Green Lentils, 16 oz bag, UPC 04149829…
- Reason
- Product may contain undeclared wheat
- Published
- May 13, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc., Bethlehem, PA 18018-3524, NDC 0264-3145-11
- Reason
- Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
- Published
- May 6, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Esomeprazole Magnesium Delayed Release Capsules USP, 40 mg*, 1000-count bottles, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 INDIA, NDC 43598-510-10
- Reason
- Discoloration: product contains brown pellets
- Published
- May 6, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Nizatidine Oral Solution, 15 mg/mL (75 mg/5mL) USP 480 mL bottles, Rx Only Distributed by: Gemini Laboratories, LLC Bridgewater, NJ 08807 NDC 60846-301-15
- Reason
- CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.
- Published
- May 6, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
WHOLE FOODS MARKET
- Product
- Whole Foods Market Minestrone Soup PLU code printed on the p…
- Reason
- May contain undeclared milk
- Published
- May 6, 2020
- Distribution
- Alabama, Arizona, California, Colorado,…
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.
