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
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.
36,950
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,732
Class I recallsReasonable probability of serious health consequences24,263
Class II recallsTemporary or medically reversible health consequences2,873
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
2,071 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.
Filters
Metric
View
A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,458 recalls have been announced year to date.
- Aug 2026 was 53% 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 | 24,263 |
| Class I | 9,732 |
| Class III | 2,873 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,263 |
| Class I | 9,732 |
| Class III | 2,873 |
| Not Yet Classified | 1 |
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
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 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
FDA Recall Ongoing 2026 recordClass III
parodontax (cetylpyridinium chloride)ACTIVE GUM HEALTH, Mouthwash, Mint. Net Wt 16.9 FL OZ (500 mL), Distributed by Haleon, Warren, NJ 07059. NDC 0135-0651-02
- Reason
- Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
- Published
- February 4, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015 NDC: 0338-0004-02.
- Reason
- Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution
- Published
- February 4, 2026
- Distribution
- Nationwide
FDA Recall United States Completed 2026 recordClass I
SUPERFOODS, INC.
- Product
- a.) Live it Up brand Super Greens; Natural Wild Berry Flavor…
- Reason
- Products may be contaminated with Salmonella Typhimurium
- Published
- February 4, 2026
- Distribution
- Nationwide
FDA Recall United States Completed 2026 recordClass I
SUPERFOODS, INC.
- Product
- Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgr…
- Reason
- Products may be contaminated with Salmonella Typhimurium
- Published
- February 4, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Icosapent Ethyl capsules, 1 gram, 120-count bottles, Rx only, Manufactured by: Softgel Healthcare Pvt. Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 70710-1592-07
- Reason
- Subpotent Drug: Due to oxidation caused by leakage of the contents of the capsules
- Published
- January 28, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Thyroid, USP, Rx only, Net Wt: 0.50kg, For Manufacturing, Processing or Repackaging Use Only, Specialty Process Labs, Phoenix, AZ 85034, NDC 81305-100-02
- Reason
- Subpotent Drug
- Published
- January 28, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Furosemide Tablets, USP 40 mg, 1,000 Tablets, Rx Only, Manufactured for: Rising Pharmaceuticals Inc., East Brunswick, NJ 08816, Manufactured by: Graviti Pharmaceuticals Pvt. Ltd. Telangana - 502307, India, NDC 64980-563-10.
- Reason
- Presence of Foreign Substance
- Published
- January 28, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass III
Diclofenac Sodium Topical Gel, 1%, NET WT 100 g (3.53 oz), Manufactured by: DPT Laboratories, Ltd., 307 E Josephine Street, San Antonio, TX 78215. NDC: 76282-103-39
- Reason
- Failed PH Specifications
- Published
- January 28, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Lanreotide Injection, 120 mg/0.5 mL, 0.5 mL per pre-filled syringe, For deep subcutaneous injection, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-870-67
- Reason
- Presence of Particulate Matter.
- Published
- January 21, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGATE, MAXFRESH, SPICY FRESH, RED TOOTH PASTE, 72CT, 150G; e) CREST, TOOTHPASTE, 40CT, 8.2OZ, UPC: 037000247081
- Reason
- CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
- Published
- January 21, 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.
