FDA Recall United States Terminated Historical recordClass II
Morski Brands, Inc.
- Product
- Steakhouse Potato Salad, Keep Refrigerated packaged in the f…
- Reason
- Foreign object (metal).
- Published
- June 22, 2022
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,113
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/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 | 24,343 |
| 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
Taylor Farms New Jersey, Inc.
- Product
- Wawa Apples & Peanut Butter 4.9oz. snack
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Product shipped to distributor in NJ the…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Peanut Butter Fudge 8 oz. Item code: K509
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Peanut Butter and Chocolate Fudge 8 oz. Item code: K508
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Milk Chocolate Covered Peanut Butter Ritz Crackers 8 pieces.…
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Milk Chocolate Covered Peanut Butter Meltaways 8oz. Item cod…
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Dark Chocolate Covered Peanut Butter Meltaways 8oz. Item cod…
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Milk Chocolate Covered Peanut Butter Eggs - 8 oz. Box Item c…
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall United States Terminated Historical recordClass I
Cargill Cocoa and Chocolate Inc
- Product
- Dark Chocolate Covered Peanut Butter Eggs - 8 oz. Item code:…
- Reason
- Possible contamination with Salmonella
- Published
- June 22, 2022
- Distribution
- Retail store in PA. Consumers in PA, S…
FDA Recall Terminated Historical recordClass II
Paracentesis/Thoracentises Tray (10/cs) Rx CRFPED, Lidocaine Hydrochloride USP, 1%, 5mL, Rx only, MFG: Becton Dickinson
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Biopsy and Aspiration Tray Bone Marrow Illinois 11GX4 (10/cs) Rx CRFPED Lidocaine Hydrochloride USP, 1%, 5mL, Rx only, MFG: Becton Dickinson
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Intralipid (I.V. Fat emulsion), 20%, 100 mL bag, Rx only, MFG: Baxter Healthcare, NDC 0338-0519-58
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Intralipid (I.V. Fat emulsion), 20%, 250 mL bag, Rx only, MFG: Baxter Healthcare, NDC 0338-0519-09
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Cefazolin for injection USP, and Dextrose Injection, USP, 2 g, 50 mL duplex container, Rx only, MFG: B. Braun Medical Inc., NDC 0264-3105-11
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Cefazolin for injection USP, and Dextrose Injection, USP, 1G, 50 ML duplex container, Rx only, MFG: B. Braun Medical Inc., NDC 0264-3103-11
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diprivan (Propofol) Emulsion, 200 mg per 20 mL (10mg/mL), 20 mL vial, Rx only, MFG: App Pharmaceutical LLC, NDC 63323-269-29
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diprivan (Propofol) Emulsion, 100 mg/mL, 10mL vial, Rx only, MFG: App Pharmaceutical LLC, NDC 63323-269-10
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ofloxacin Otic Solution 0.3%, 5 mL bottle, Rx only, MFG: Amneal/Akyma Pharmaceuticals, NDC 69238-1615-3
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Tetracaine Hydrochloride Ophthalmic Solution, 0.5%, 4 mL bottle, Rx only, MFG: Alcon Surgical Inc., NDC 0065-0741-14
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Geodon for injection (ziprasidone mesylate), 20 mg/mL, 1 mL single dose vial, Rx only, MFG: Viatris, NDC 0049-3920-83
- Reason
- cGMP deviations: Temperature abuse
- Published
- June 15, 2022
- 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.
