FDA Recall United States Ongoing 2026 recordClass II
Tom Bumble LLC
- Product
- Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Cho…
- Reason
- Foreign material.
- Published
- January 7, 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.
37,060
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
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 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 | 24,313 |
| 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 Ongoing Historical recordClass II
Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension, 300 mg, 8 packets per carton, Rx Only, Manufactured for: Merck Sharp & Doohme LLC, Rahway, NJ 07056 USA, Manufactured by: N.V. Organon, 5349 AB Oss, The Netherlands, a subsidiary of Organon & Co., Jersey City, NJ 07302, USA NDC 0085-2224-02.
- Reason
- Presence of particulate matter: potential presence of metal particulates in the product.
- Published
- December 31, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Merck Emend (aprepitant) for oral suspension, 125 mg, Single-Dose Kit, Rx Only, Manufactured for: Merck Sharpe & Dohme LLC, Rahway, NJ 07065, USA, Manufactured by: Novo Nordisk Production Ireland Limited Athlone, Ireland, NDC 0006-3066-03
- Reason
- Presence of particulate matter: potential presence of metal particulates in the product.
- Published
- December 31, 2025
- Distribution
- Nationwide
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Sinus Cap Herbal Supplement, Herbs containing antibiotic, dr…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Pain Away Herbal Supplement, Analgesic & anti-inflammatory p…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Organic Ginger Root Herbal Supplement, Natural anti-inflamma…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Ear Drops Herbal Supplement, Mullein flower alcohol tincture…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Ext…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Baby Soothe Herbal Supplement, Promotes rest, helps ease col…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Ongoing Historical recordClass II
A New Life Herbs, LLC
- Product
- Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to…
- Reason
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Published
- December 31, 2025
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Silvestri Sweets Inc dba Carousel Candies
- Product
- Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz.…
- Reason
- Undeclared pecan
- Published
- December 31, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Silvestri Sweets Inc dba Carousel Candies
- Product
- Choceur Pecan Cranberry & Cinnamon Holiday Bark. Standup Pou…
- Reason
- Undeclared wheat
- Published
- December 31, 2025
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Mondelez Global Llc
- Product
- Ritz Peanut Butter Cracker Sandwiches, Net Wt. 27.6 oz.- 20…
- Reason
- Undeclared allergens (Peanut) due to mispackaging
- Published
- December 31, 2025
- Distribution
- The recalled product was distributed to…
FDA Recall Ongoing Historical recordClass II
Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08
- Reason
- Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
- Published
- December 24, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Cisatracurium Besylate Injection USP, 20 mg/10 mL*,(2 mg/mL), 10 x 10 mL Multiple-dose Vials per carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, 10mL Multiple-dose vial, NDC 70069-161-01; 10x10mL Multiple-dose vials per Carton, NDC 70069-161-01.
- Reason
- Subpotent product:out of specification assay results observed during long term stability testing.
- Published
- December 24, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Cisatracurium Besylate Injection USP, 200mg/20mL*(10mg/mL), 10 x 20 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single dose 20mL vial NDC 70069-151-01; 10 x 20 Single dose vials per Carton, NDC 70069-151-10.
- Reason
- Subpotent product:out of specification assay results observed during long term stability testing.
- Published
- December 24, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Cisatracurium Besylate Injection USP, 10 mg/5 mL* (2mg/mL), 10 x 5 mL Single-dose Vials per Carton, Rx Only, Manufactured for: Somerset Therapeutics, LLC, Hollywood, FL 33024, Made in India, Single-dose 5 mL vial NDC 70069-141-01; 10x5 mL single dose vial per Carton NDC 70069-141-10.
- Reason
- Subpotent product:out of specification assay results observed during long term stability testing.
- Published
- December 24, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Baclofen Tablets USP, 10 mg, 1000-count bottles, Rx only, Marketed by: GSMS, Incorporated, CA 93012 USA. NDC 51407-973-10
- Reason
- Presence of Foreign Tablets/Capsules
- Published
- December 24, 2025
- 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.
