FDA Recall United States Terminated Historical recordClass II
Morski Brands, Inc.
- Product
- Dawn's Campfire BBQ Beans, #90125, Net Wt 8 lb (3.63 kg) K…
- Reason
- Foreign object (metal).
- Published
- June 22, 2022
- 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
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 II
Morski Brands, Inc.
- Product
- Marketside Gouda Bacon Green Chile Dip, Net Wt 12 oz. (340…
- Reason
- Foreign object (metal).
- Published
- June 22, 2022
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Morski Brands, Inc.
- Product
- Ranch BLT Pasta Salad, Keep Refrigerated packaged in the fol…
- Reason
- Foreign object (metal).
- Published
- June 22, 2022
- Distribution
- Nationwide
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
FDA Recall United States Terminated Historical recordClass II
THISTLE HEALTH INC
- Product
- Thistle Tropical Limeade Cold-Pressed Organic Juice watermel…
- Reason
- Manufactured using organic strawberries potentially contaminated with Hep A.
- Published
- June 22, 2022
- Distribution
- U.S. distribution to the following: CA,…
FDA Recall United States Terminated Historical recordClass II
THISTLE HEALTH INC
- Product
- Thistle Watermelon Berry Cold-Pressed Organic Juice watermel…
- Reason
- Manufactured using organic strawberries potentially contaminated with Hep A.
- Published
- June 22, 2022
- Distribution
- U.S. distribution to the following: CA,…
FDA Recall United States Terminated Historical recordClass III
Abbott Laboratories
- Product
- Pedialyte***Replaces Electrolytes***Great for Kids and Adult…
- Reason
- The third party contract manufacturer used a dextrose ingredient derived from wheat in one lot of the Strawberry Lemonade powder, which is not declared on the label.
- Published
- June 22, 2022
- Distribution
- AZ, CA, FL, GA, IL, IN, MN, NC, NY, OH,…
FDA Recall United States Terminated Historical recordClass I
Butter Buds Inc
- Product
- Butter Buds Food Ingredients. Butter Buds 8X Non-Dairy LD,…
- Reason
- Undeclared milk.
- Published
- June 22, 2022
- Distribution
- CA, CT, IL, MN, NC, OH, WA. Outside the…
FDA Recall United States Terminated Historical recordClass I
Blue Moose of Boulder, LLC
- Product
- Blue Moose Spinach Artichoke Parmesan Dip, 7 oz. (198g), pac…
- Reason
- Spinach Artichoke Cashew Dip was mislabeled with Spinach Artichoke Parmesan Dip label and does not state that the product contains cashews and soy.
- Published
- June 22, 2022
- Distribution
- CA, OH. Note: Ohio product was destroy…
FDA Recall Terminated Historical recordClass I
Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704
- Reason
- Subpotent drug
- Published
- June 15, 2022
- Distribution
- CA
FDA Recall Terminated Historical recordClass I
Tacrolimus (Brand Capsules ) 0.5 mg/mL Suspension, Rx, This is a compounded medication., Valor Compounding Pharmacy, 2461 Shattuck Ave., Berkeley, CA 94704,
- Reason
- Subpotent drug
- Published
- June 15, 2022
- Distribution
- CA
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
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.
