FDA Recall United States Terminated Historical recordClass I
Frito-Lay, Inc
- Product
- 30 count Lays Kettle Cooked Multipack Tray 41.25 oz. package…
- Reason
- Potential presence of Salmonella
- Published
- May 17, 2017
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,135
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/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 | 24,349 |
| 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
Frito-Lay, Inc
- Product
- 30 count Miss Vickies Multipack Tray 41.25 oz. packaged in f…
- Reason
- Potential presence of Salmonella
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Frito-Lay, Inc
- Product
- 20 count Frito-Lay Bold Mix Sack 18.4 oz. packaged in flexib…
- Reason
- Potential presence of Salmonella
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Frito-Lay, Inc
- Product
- 12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged…
- Reason
- Potential presence of Salmonella
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Frito-Lay, Inc
- Product
- Jalape¿o Flavored Lays Kettle Cooked potato chips and Jalape…
- Reason
- Potential presence of Salmonella
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Treehouse Foods
- Product
- Macaroni & Cheese microwaveable cups sold under the followin…
- Reason
- Products containing cheddar cheese seasoning which may be contaminated with Salmonella.
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Pinnacle Foods, LLC
- Product
- Great Value Bread and Butter Chips 24 Fl Oz. Distributed b…
- Reason
- Glass fragments were found in Great Value Bread and Butter Chips.
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Jimmy's Cookies
- Product
- The Bakery Peanut Butter Chocolate Chunk Cookies, Net Wt. 14…
- Reason
- The Bakery Peanut Butter Chocolate Chunk Cookies may contain undeclared milk.
- Published
- May 17, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Sulfamethoxazole and Trimethoprim Oral Suspension, USP 200 mg / 40 mg per 5 mL , Grape Flavor, Rx Only, 16 fl oz. (473 mL), HI-TECH PHARMACAL CO., INIC, Amityville, NY 11701, NDC 50383-824-16
- Reason
- Failed Dissolution Specifications
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m NDC 51522-0694-5.
- Reason
- Labeling: Error on Declared Strength: Error is due to an incorrect value in the Drug Facts Panel. The correct strength is displayed on the primary container.
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Allergy Relief Diphenhydramine HCl 25 mg, Antihistamine, Dye-Free, 24 Softgels, distributed under the following labels: (a) TopCare Allergy Relief, DISTRIBUTED BY TOPCO ASSOCIATES LLC, ELK GROVE VILLAGE, IL 60007, NDC 36800-483-24, UPC 0-36800-39134-5; (b) Rexall Since 1903 Allergy Relief, PACKAGED FOR DOLGENCORP, LLC, 100 MISSION RIDGE GOODLETTSVILLE, TN 37072, UPC 3-59726-72025-0; (c) HyVee health Allergy Relief, DISTRIBUTED BY HY-VEE, INC. 5820 WESTOWN PARKWAY, WEST DES MOINES, IA 50266, NDC 42507-483-24, UPC 0-75450-12369-2; (d) up & up allergy relief, Distributed by Target Corporation, Minneapolis, MN 55403, NDC 11673-720-24, UPC 3-59726-72025-0; (e) smart sense allergy softgels, Distributed by Kmart Corporation, Hoffman Estates, IL 60179, NDC 49738-483-24, UPC 8-83967-39839-3.
- Reason
- Subpotent: This product is being recalled due to low out of specification assay results at the 9 month time point.
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Rabeprazole Sodium Delayed Release Tablets, 20 mg, a) 30-count bottle (NDC 65162-0724-03), b) 90-count bottle (NDC 65162-0724-09), Rx Only, Manufactured by Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad INDIA 382220, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ 08807
- Reason
- Failed Dissolution Specifications
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Aripiprazole Tablets, 2 mg, 30 count unit dose box, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada, Distributed by Major Pharmaceuticals, Livonia, MI NDC 0904-6509-04
- Reason
- Superpotent Drug; out of specification results for assay (manufacturer)
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
- Reason
- Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass I
EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.
- Reason
- Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fluconazole Tablets, USP, 200 mg, 100-count Unit Dose carton, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA, Distributed by MAJOR PHARMACEUTICALS, 31778 Enterprise Dr., Livonia, MI 48150 USA, NDC 0904-6501-61
- Reason
- Failed Dissolution Specifications
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Fluconazole Tablets, USP, 100 mg, 100-count Unit Dose carton, Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA, Distributed by MAJOR PHARMACEUTICALS, 31778 Enterprise Dr., Livonia, MI 48150 USA, NDC 0904-6500-61
- Reason
- Failed Dissolution Specifications
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Threshold Enterprises Ltd
- Product
- Source Naturals Dietary Supplement Vitamin D-3; Bioactive…
- Reason
- Testing of Vitamin D-3 as a result of a consumer complaint found specific lots to have lower concentrations than product specifications of ingredient labeling.
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Weaver Popcorn Co.
- Product
- Trail's End Chicago Cubs Sweet and Savory Collection Trai…
- Reason
- Product has the potential to be contaminated with Salmonella
- Published
- May 10, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Phenylephrine 2.5%, Tropicamide 1%, 15 mL Multi-Dose Ophthalmic (spelled Opthalmic) Drops in a bottle, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1300, barcode 3 70285 13001 4.
- Reason
- Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.
- Published
- May 3, 2017
- 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.
