FDA Recall United States Terminated Historical recordClass II
Freshbev LLC
- Product
- KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce
- Reason
- Elevated patulin levels.
- Published
- April 5, 2017
- 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.
37,204
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,841
Class I recallsReasonable probability of serious health consequences24,366
Class II recallsTemporary or medically reversible health consequences2,892
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
2,073 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 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)
- 1,714 recalls have been announced year to date.
- Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
- The highest complete period was Jun 2026 (297).
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
| Class | Recalls |
|---|---|
| Class II | 24,366 |
| Class I | 9,841 |
| Class III | 2,892 |
| Not Yet Classified | 2 |
FDA Recall United States Terminated Historical recordClass II
Freshbev LLC
- Product
- Apple Juice 5 Gal, Keep Refrigerated, Ripe Liquid Produce
- Reason
- Elevated patulin levels.
- Published
- April 5, 2017
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Azteca Milling LP
- Product
- Tortilla Chip 2 White Corn Masa Flour 50 lb bags
- Reason
- The firm stated that they were notified by some of their customers that their product contains metal fragments.
- Published
- April 5, 2017
- Distribution
- Product was distributed in the following…
FDA Recall United States Terminated Historical recordClass II
Azteca Milling LP
- Product
- Tortilla Chip #8 Especial White NGMO Corn Masa Flour 50 lb b…
- Reason
- The firm stated that they were notified by some of their customers that their product contains metal fragments.
- Published
- April 5, 2017
- Distribution
- Product was distributed in the following…
FDA Recall United States Terminated Historical recordClass II
Azteca Milling LP
- Product
- Taco 6 White NGMO Corn Masa Flour 50 lb bags
- Reason
- The firm stated that they were notified by some of their customers that their product contains metal fragments.
- Published
- April 5, 2017
- Distribution
- Product was distributed in the following…
FDA Recall United States Terminated Historical recordClass II
Azteca Milling LP
- Product
- Taco 4 Blue Corn Masa Flour 50 lb bags
- Reason
- The firm stated that they were notified by some of their customers that their product contains metal fragments.
- Published
- April 5, 2017
- Distribution
- Product was distributed in the following…
FDA Recall United States Terminated Historical recordClass II
Azteca Milling LP
- Product
- Truco 1 50/50 Corn Masa Flour 50 lb bags & totes
- Reason
- The firm stated that they were notified by some of their customers that their product contains metal fragments.
- Published
- April 5, 2017
- Distribution
- Product was distributed in the following…
FDA Recall United States Terminated Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- The Bakery Mini Pecan Tarts Part Platter NET WT 16x 16.2 OZ…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Pecan Tarts Party Platter 16 x 16.2 (460g) item num…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Turtle Brownie Party Platter 16 x 12.2 oz (346g) it…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass III
Give and Go Prepared Foods Corp - Finch
- Product
- Two-Bite Pecan Tart 9.2 oz (261g) item number 02023; NL Two-…
- Reason
- Dried weevil larvae may be present in the recalled products.
- Published
- April 5, 2017
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Bitterman and Sons
- Product
- Parmesan Truffle Salt. The product is packaged in glass tast…
- Reason
- Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on label.
- Published
- April 5, 2017
- Distribution
- distributed in AK, CA, CT, FL, IL, IN, K…
FDA Recall Terminated Historical recordClass II
Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60
- Reason
- Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40
- Reason
- Presence of Particulate Matter
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13
- Reason
- Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).
- Reason
- Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
- Published
- March 29, 2017
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.
- Reason
- Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
- Published
- March 29, 2017
- 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.
