FDA Recall United States Ongoing 2026 recordClass II
Diva Fam Inc
- Product
- Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
- Reason
- potential Clostridium botulinum contamination
- Published
- February 11, 2026
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,059
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,786
Class I recallsReasonable probability of serious health consequences24,313
Class II recallsTemporary or medically reversible health consequences2,876
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
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 | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,313 |
| Class I | 9,786 |
| Class III | 2,876 |
| Not Yet Classified | 2 |
FDA Recall United States Ongoing 2026 recordClass II
Diva Fam Inc
- Product
- Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
- Reason
- potential Clostridium botulinum contamination
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass II
Diva Fam Inc
- Product
- Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
- Reason
- potential Clostridium botulinum contamination
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass II
Diva Fam Inc
- Product
- Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
- Reason
- potential Clostridium botulinum contamination
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass II
Diva Fam Inc
- Product
- Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individuall…
- Reason
- potential Clostridium botulinum contamination
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass II
Organic Spices, Inc
- Product
- spicely ORGANIC sumac NO ARTIFICIAL COLORING NO GLUTEN - NO…
- Reason
- Product contains salt and is mislabeled
- Published
- February 11, 2026
- Distribution
- U.S. Distribution: CA, CO, IL, IN, MI, N…
FDA Recall United States Ongoing 2026 recordClass II
Organic Spices, Inc
- Product
- spicely ORGANIC celery salt NO ARTIFICIAL COLORING NO GLUTE…
- Reason
- Product contains salt and is mislabeled
- Published
- February 11, 2026
- Distribution
- U.S. Distribution: CA, CO, IL, IN, MI, N…
FDA Recall United States Ongoing 2026 recordClass II
Organic Spices, Inc
- Product
- spicely ORGANIC garlic salt NO ARTIFICIAL COLORING NO GLUTE…
- Reason
- Product contains salt and is mislabeled
- Published
- February 11, 2026
- Distribution
- U.S. Distribution: CA, CO, IL, IN, MI, N…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, cashew coffee milk
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, cashew milk
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, spicy lemonade
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, upbeat
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, pineapple mint
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, sweet greens
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass I
Everpress Juice
- Product
- JUICE from the Raw, DETOX GREENS
- Reason
- Under-processed product may contain pathogenic bacteria that could harm to humans.
- Published
- February 11, 2026
- Distribution
- The adulterated product was distributed…
FDA Recall United States Terminated 2026 recordClass II
Winco Foods Llc
- Product
- WinCo Foods Deli Margherita Pizza Thin Crust, Item #67279. N…
- Reason
- Product may contain foreign material (metal fragments).
- Published
- February 11, 2026
- Distribution
- Distributed in AZ, CA, ID, MT, NV, OK, O…
FDA Recall United States Completed 2026 recordClass III
Optiwize Inc.
- Product
- OptiWize Health OptiWize Collagen Plus 320 count bottle; W…
- Reason
- The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity.
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall United States Ongoing 2026 recordClass III
Fazt & Loud LLC
- Product
- Lost and Found Energy, Sour Gummy Bear, 12pck, 16oz Cans Cas…
- Reason
- Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
- Published
- February 11, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass III
Glycopyrrolate Oral Solution, 1 mg/5 mL, 16 oz. (473 mL), Rx only, Manufactured by: MSN Pharmaceuticals Inc., Piscataway, NJ 08854, Distributed by: Novadoz Pharmaceuticals LLC, Piscataway, NJ 08854, NDC 72205-070-72
- Reason
- Failed Impurities/Degradation Specifications
- Published
- February 4, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2
- Reason
- Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
- Published
- February 4, 2026
- 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.
