FDA Recall United States Terminated 2026 recordClass II
ZIYAD BROTHERS IMPORTING
- Product
- Baraka Gourmet Pastry Kunafe 6.7oz., UPC 822514291060, 18 re…
- Reason
- May contain partially hydrogenated oils
- Published
- January 14, 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 United States Terminated 2026 recordClass II
ZIYAD BROTHERS IMPORTING
- Product
- Baraka French Style Puff Pastry 1lb and 1.5lbs sizes, UPCs 8…
- Reason
- May contain partially hydrogenated oils
- Published
- January 14, 2026
- Distribution
- Nationwide
FDA Recall United States Terminated 2026 recordClass II
McCain Foods USA Inc
- Product
- Sysco Imperial Potato Tater Barrel, item number 1000006067.…
- Reason
- Clear hard plastic fragments.
- Published
- January 14, 2026
- Distribution
- Distributed in AK, AZ, CA, CO, FL, HI, I…
FDA Recall United States Terminated 2026 recordClass II
McCain Foods USA Inc
- Product
- Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. F…
- Reason
- Clear hard plastic fragments.
- Published
- January 14, 2026
- Distribution
- Distributed in AK, AZ, CA, CO, FL, HI, I…
FDA Recall United States Terminated 2026 recordClass I
Lund Food Holdings Inc
- Product
- Lunds & Byerlys Monster Cookies, Net Wt 10.0 oz (284g).. UPC…
- Reason
- Undeclared allergens (Peanut, Egg, Soy)
- Published
- January 14, 2026
- Distribution
- MN
FDA Recall United States Ongoing 2026 recordClass II
Town Food Service Equip Co Inc
- Product
- Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1Q…
- Reason
- Product found to contain leachable lead levels.
- Published
- January 14, 2026
- Distribution
- AL, AR, AZ, CA, CO, FL, GA, IL, KY, LA,…
FDA Recall Ongoing 2026 recordClass III
traZODONE Hydrochloride Tablets, USP, 100mg, 1,000 Tablets, Rx only, Manufactured by: Zydus Lifesciences Ltd., India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534, NDC 68382-806-10
- Reason
- Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.
- Published
- January 7, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Ondansetron Orally Disintegrating Tablets, USP, 4mg, 30 Tablets (3 blistercards each containing 10 tablets), Rx only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430, Product of India, NDC 68462-157-13
- Reason
- Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out. Preferred Pharmaceuticals purchased the finished product and repackaged the product for sale.
- Published
- January 7, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4501-14
- Reason
- Presence of Particulate Matter: Hair was found in a prefilled syringe
- Published
- January 7, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Bagsvaerd, Denmark, Product of Denmark, Novo Nordisk A/S, Novo Nordisk Inc., Plainsboro, NJ 08536, NDC 0169-4505-14
- Reason
- Presence of Particulate Matter: Hair was found in a prefilled syringe
- Published
- January 7, 2026
- Distribution
- Nationwide
FDA Recall Ongoing 2026 recordClass II
BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL Applicator, CareFusion 213, LLC, El Paso, TX 79912, NDC 54365-401-29
- Reason
- Lack of Assurance of Sterlity
- Published
- January 7, 2026
- Distribution
- Nationwide
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
FDA Recall United States Terminated 2026 recordClass III
Bendon Publishing
- Product
- 1) Paw Patrol Heart-Shaped Gummy Candies, Mixed Fruit, Net W…
- Reason
- Unapproved color additive - chlorophyllin copper complex
- Published
- January 7, 2026
- Distribution
- Distributors in FL, MN, TX, WA
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
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.
