FDA Recall United States Terminated Historical recordClass II
Starwest Botanicals, Inc
- Product
- Starwest Botanicals Item#: 209617-34, Item# 209617-31 Woo…
- Reason
- Presence of E. coli species
- Published
- April 21, 2021
- Distribution
- Nationwide
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.
37,113
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
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 | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall Terminated Historical recordClass II
Neomycin Sulfate Tablets, USP 500mg, Rx Only, 10x10 Unit dose 100 Tablets, Manufactured for: X-GEN Phamaceuticals, Inc. Big Flats, NY 14814. NDC 39822-0310-5
- Reason
- Failed Stability Specifications: Out of Specification (OOS) result reported for microbiological assay
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Mometasone Furoate Topical Solution, USP, 0.1%, (Lotion), a) 30 mL (NDC 0713-0701-85) and b) 60 mL (NDC 0713-0701-53), Rx Only, Distributed by: Cosette Pharmaceuticals, Inc., South Plainfield, NJ 07080
- Reason
- CGMP Deviaitons
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division) Panelav 38935, Gujarat, India Manufactured for: Alembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807, NDC 62332-087-30
- Reason
- Labeling: Label-mixup
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Metformin HCl Extended-Release Tablets, USP, 500 mg, Rx Only, 500-count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Industries Ltd., Halol-Baroda HIghway, Halol-389 350 Gujarat, India, NDC 62756-142-02.
- Reason
- Failed Moisture Limits: Out of specification for water content
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Ongoing Historical recordClass II
Guanfacine Extended-Release Tablets 2 mg,100-count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-3928-1, UPC 3 60505 39281 0
- Reason
- Cross Contamination with Other Product: Product is being recalled due to Trace Amounts of Quetiapine Fumarate
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199 Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5 UPC 0 36000 91592 1
- Reason
- Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are incorrectly labeled as Moisturizing Foam Hand Sanitizer
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
Sea World, LLC
- Product
- Crimson Snapper Fillet, Natural Cut CO Treated, Net WT 10 LB…
- Reason
- Fish decomposition.
- Published
- April 14, 2021
- Distribution
- Domestic distribution only-PR
FDA Recall United States Terminated Historical recordClass III
New Generation Wellness Inc.
- Product
- VEGAN VITAMIN D3, 50 mcg (2,000 IU), 60 VEGAN TABLETS in 100…
- Reason
- Vitamin D3 stability sample analyzed and found to be less than 100% of label claim.
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
New Generation Wellness Inc.
- Product
- Live Better vegan vitamin d-3 by CVS Health, 50 mcg (2000 IU…
- Reason
- Vitamin D3 stability sample analyzed and found to be less than 100% of label claim.
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Simply Delicious Inc.
- Product
- Bobo's Maple Pecan Oat Bars, 3 oz., UPC 8 2926200021 0, Best…
- Reason
- Two consumer complaints were received for peanuts in maple pecan bars.
- Published
- April 14, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
ZOMA-Jet 10 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 10 mg vial, ZOMA-Jet 10 Demonstration Kit contains -ZOMA-Jet 10 device - 7 Needle-Free Head A's - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054; UPC 3 55566 19031 4.
- Reason
- Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
ZOMA-Jet 5 Demonstration Kit, Needle-free delivery device for use with ZOMACTON (somatropin) for injection 5mg vial, Rx only, ZOMA-Jet 5 Demonstration Kit contains -ZOMA-Jet 5 device - 5 Needle-Free Head A's - 2 Vial Adaptors - 1 Carrying Case - 1 User Manual; Manufactured for: Ferring Pharmaceuticals Inc. Parsippany, NJ 07054; UPC 3 55566 18031 5.
- Reason
- Defective Delivery System: customer complaints concerning the injector pen breaking apart and disintegrating into pieces.
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01, For Intravenous Infusion Only MUST BE DILUTED PRIOR TO USE, packaged in 10 x 10mL Single-Dose Vials per pack NDC 68382-048-10, Rx only, Manufactured by: Cadila Healthcare Ltd., Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534.
- Reason
- Crystallization: customer complaints for crystallization in finished product.
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01, For Intravenous Infusion Only MUST BE DILUTED PRIOR TO USE, packaged in 10 x 20mL Single-Dose Vials per pack NDC 68382-049-10, Rx only, Manufactured by: Cadila Healthcare Ltd., Vadodara, India. Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534.
- Reason
- Crystallization: customer complaints for crystallization in finished product.
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Nuts.com
- Product
- Nuts.com brand Diced Dried Figs packaged in 1lb stand up gus…
- Reason
- Undeclared almonds in diced fig product
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Wilton Industries Inc
- Product
- Holiday Home Assorted Treat Toppings, 2.6oz (74g) 3 hanging…
- Reason
- Undeclared milk
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Wilton Industries Inc
- Product
- Wilton Autumn Assorted Treat Toppings Sprinkles, 2.6oz (74g)…
- Reason
- Undeclared milk
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Wilton Industries Inc
- Product
- Wilton Rainbow Chip Crunch Sprinkles, 5.25oz (148g) clear pl…
- Reason
- Undeclared milk
- Published
- April 7, 2021
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Wilton Industries Inc
- Product
- Wilton Holiday Mix Sprinkles, 7.6oz (215g) clear plastic bot…
- Reason
- Undeclared milk
- Published
- April 7, 2021
- 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.
