FDA Recall United States Terminated Historical recordClass II
Pepsico Inc
- Product
- Starbucks frappuccino Vanilla. Chilled Coffee Drink. 13.7 F…
- Reason
- Foreign object (glass).
- Published
- February 22, 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
Posaconazole Delayed-Release Tablets, 100 mg, 60-count bottle, Rx Only, Manufactured for: Biocon Pharma Inc., Iselin, NJ 08830-3009; Manufactured by: Biocon Pharma Limited, Bengaluru, India - 560 099, NDC 70377-038-11.
- Reason
- Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass III
Atropine Sulfate Ophthalmic Solution, USP 1%, For Topical Application To The Eye, 2 mL bottle, Sterile, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. NDC: 17478-215-02
- Reason
- Failed Stability Specifications: Out of specification test results for viscosity was identified at the 12M stability timepoint.
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ohm Sanitizer Spray (alcohol (ethyl alcohol) 80% v/v, 8 FL OZ (237 ML) bottles.
- Reason
- CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Ohm Hand Sanitizer (alcohol (ethanol) 70 % v/v), packaged in a) 2 FL OZ (60 ML), b) 3 FL OZ (88 ML) bottles, c) 10 FL OZ (295 ML) bottles, d)12 FL OZ (355 ML) bottles, e)16 FL OZ (473 ML) bottles, f) 64 FL OZ (1892 ML) bottles, g) 128 FL OZ (3785 ML) bottles
- Reason
- CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Mondelez Global Llc
- Product
- Sour Patch Kids Watermelon Jelly Beans Net Wt.3 OZ (368g) UP…
- Reason
- Undeclared FD&C Yellow No. 5
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Ortho Molecular Products, Inc.
- Product
- Fiber Powder, Dietary Supplement, Apple Cinnamon Flavored, p…
- Reason
- Raw material tested positive for Cronobacter sakazakii.
- Published
- February 15, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Diltiazem Hydrochloride Extended-Release Capsules, USP, 360 mg; Rx only; 90-count bottles, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway, Halol-389350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, NDC 47335-679-81
- Reason
- Failed Impurity (Deacetyl Diltiazem Hydrochloride) specification during stability testing and failed dissolution testing at FDA laboratory.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2131
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
CVS First Aid Home, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 2980-0700
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2132
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care First Aid Class A ANSI 25 Person, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2150
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care First Aid 10 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2128
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care First Aid 25 Person 2009 ANSI, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 9999-2129
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Adventure First Aid 1.5, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0212
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Adventure First Aid 1.0, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 0120-0213
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Adventure Marine 150, First Aid Kit, containing Easy Care first aid After Burn Cream 0.9 g packets, Product # 1015-0150
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and lidocaine hydrochloride 0.5%), 0.9 g (0.03 oz) packets packaged in boxes of 10, Treatment for Burns, Made in China for Adventure Ready Brands, 944 Industrial Park Rd., Littleton, NH 03561, NDC 90107-0210, Product # 9999-1515
- Reason
- Microbial Contamination of Non-Sterile Products: FDA Laboratory results found product to be contaminated with Bacillus lichenformis and Bacillus sonorensis.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Professional Complementary Health Formulas, LLC
- Product
- Vitamin B Complex packaged in white plastic bottle labeled i…
- Reason
- Product recalled due to undeclared niacin.
- Published
- February 8, 2023
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Professional Complementary Health Formulas, LLC
- Product
- Inositol packaged in white plastic bottle with UPC 406511156…
- Reason
- Product recalled due to undeclared niacin.
- Published
- February 8, 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.
