FDA Recall United States Terminated Historical recordClass II
CELEBRATION HERBALS US
- Product
- Celebration Herbals Senna Leaf Herbal Tea 24 Teabags, net wt…
- Reason
- possible salmonella
- Published
- December 24, 2025
- Distribution
- Multiple states
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.
37,060
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.
Filters
Metric
View
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
Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.
- Reason
- Defective container - seal not adhering to bottles
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-412-02
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-411-02
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only, Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC: 69097-410-02
- Reason
- CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL), 30 mL, Rx Only, For Oral Use Only, Manufactured By: /winder Laboratories, LLC, Winder, GA 30680. NDC: 75826-131-01
- Reason
- Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, Madhya Pradesh 454775, India, Manufactured for Avkare, Pulaski, TN 38478, Product of Italy, NDC 42291-874-90.
- Reason
- Cross Contamination with Other Products
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution, 0.5mL Single-Use Syringe, For Topical Ophthalmic Use Only. Not for IV Use. Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67226. NDC: 71266-8240-01
- Reason
- Incorrect Product Formulation
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Varenicline Tablets, 1mg, 56 Tablets, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 43598-908-56
- Reason
- Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., (a subsidary of Cipla Ltd) Hauppauge, NY 11786, Manufactured for: Exelan Pharmaceuticals, Inc., Boca Raton, FL 33422, Carton NDC 76282-478-90; Bottle NDC 76282-478-13.
- Reason
- Failed stability specifications: Out of specification for hardness test
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Lanthanum Carbonate chewable tablets, 1000mg*, 10x9 bottles per patient pack carton, Rx Only, Manufactured by: Invagen Pharmaceuticals, Inc., Hauppauge, NY 11786, Manufactured for : Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-936-98.
- Reason
- Failed stability specifications: Out of specification for hardness test
- Published
- December 17, 2025
- Distribution
- Nationwide
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- Sticker label (for Loose Bulk - peppermint peaches): 4401
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- Sticker label (for Loose Bulk - peppermint peaches): 4401
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- Sticker label (for Loose Bulk - white peaches): 4401
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- Sticker label (for Loose Bulk - yellow peaches): 4044
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- Sticker label (for Loose Bulk - yellow peaches): 4044
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUN…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET W…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE O…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
FDA Recall United States Completed Historical recordClass I
Moonlight Packing Corporation
- Product
- UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A. NET WT 2 LB (3…
- Reason
- Potential contamination with Listeria monocytogenes.
- Published
- December 17, 2025
- Distribution
- Domestic: AL, AR, AZ, CA, CO, CT, FL, GA…
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.
