FDA Recall Terminated Historical recordClass II
SnoreStop Naso Spray Bulk, liquid, Distributed by Green Pharma, NDC 61152-199-99
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
Data Explorer
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,066
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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 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 Terminated Historical recordClass II
DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Babelyn Diarrhea Drops Homeopathic Remedy, 0.5 fl. oz. (15 mL) bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-035-01
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Bebelyn Colic Drops Homeopathic Remedy, 0.5 FL Oz (15 mL) bottles, distributed by Pharmadel LLC Georgetown, DE NDC 55758-036-01
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Kanjo Homeopathic Pain Relief Cream With Arnica, NET WT 2 oz (56.70G), Manufactured For: Acutens, Inc., Sheridan, WY NDC 80551-201-02
- Reason
- cGMP deviations
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Endometrin (progesterone) Vaginal Insert 100mg, packaged in a carton of 21 vaginal inserts with 21 disposable vaginal applicators, Manufactured for: Ferring Pharmaceuticals Inc., Parsippany, NJ NDC# 55566-6500-03
- Reason
- cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Tramadol Hydrochloride Tablets, USP 50 mg, Unit Dose 100-Count Tablets Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-7179-61
- Reason
- Packaging defect: blister packaging inadequately sealed.
- Published
- July 5, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Richin Trading Inc
- Product
- Sun Wave Brand Jelly Cup (Lychee Flavor); Made in Taiwan; It…
- Reason
- Potential choking hazard
- Published
- July 5, 2023
- Distribution
- Distributed to locations in AZ, CA, CO,…
FDA Recall United States Terminated Historical recordClass I
Richin Trading Inc
- Product
- Sun Wave Brand Jelly Cup (Mango Flavor); Made in Taiwan; Ite…
- Reason
- Potential choking hazard
- Published
- July 5, 2023
- Distribution
- Distributed to locations in AZ, CA, CO,…
FDA Recall United States Terminated Historical recordClass I
Richin Trading Inc
- Product
- Sun Wave Brand Jelly Cup (Assorted Flavors); Made in Taiwan;…
- Reason
- Potential choking hazard
- Published
- July 5, 2023
- Distribution
- Distributed to locations in AZ, CA, CO,…
FDA Recall United States Terminated Historical recordClass III
Anatox Inc
- Product
- Sonne's Detoxificant #7, 1 quart (946 mL) packaged in amber…
- Reason
- Elevated lead levels
- Published
- July 5, 2023
- Distribution
- Distributors, retailers, and consumers i…
FDA Recall United States Terminated Historical recordClass III
Anatox Inc
- Product
- 1. VIT-RA-TOX Calphonite #38, 15 Fl. oz. (444 ml) in an ambe…
- Reason
- Elevated lead levels
- Published
- July 5, 2023
- Distribution
- Distributors, retailers, and consumers i…
FDA Recall Terminated Historical recordClass I
ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg, Unit Dose Carton 40 Capsules, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited Bachupally-500 090 India, Distributed by: Major Pharmaceuticals Livonia, MI 48152 USA, NDC 0904-6269-08
- Reason
- Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone Hydrochloride Capsules, 20 mg were found to contain blister packages labeled as and containing Dronabinol Capsules, USP, 2.5 mg.
- Published
- June 28, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Glycopyrrolate Tablets, USP, 1 mg, 100-count bottles, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01
- Reason
- Failed Impurities/Degradation Specifications
- Published
- June 28, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
ENTRINSIC HEALTH SOLUTION INC
- Product
- enterade Advanced Oncology Formula; Original Vanilla Flavor;…
- Reason
- Potential for the product to develop mold and spoil.
- Published
- June 28, 2023
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass I
Aquamar Inc
- Product
- Kanimi Crab Flavored Seafood Fancy Shred Style 92410 Ingredi…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
FDA Recall United States Terminated Historical recordClass I
Aquamar Inc
- Product
- Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
FDA Recall United States Terminated Historical recordClass I
Aquamar Inc
- Product
- Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ing…
- Reason
- Product found to contain undeclared wheat and eggs
- Published
- June 28, 2023
- Distribution
- U.S. distribution to the following: AZ,…
FDA Recall Ongoing Historical recordClass III
Tranexamic Acid USP Tablets, 650 mg, 30 tablets (3X10) Unit Dose, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-772-13
- Reason
- Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
- Published
- June 21, 2023
- 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.
