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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to October 2026.

37,344
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,860
Class I recallsReasonable probability of serious health consequences
24,450
Class II recallsTemporary or medically reversible health consequences
2,901
Class III recallsNot likely to cause adverse health consequences

Quick 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 2,095 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitality-works-inc-recalls-365-whole-foods-market-ashwagandha-capsules-sold-nationwide-due-potentialPublished October 30, 2026
Most affected stateHawaii 200 recalls mention this state

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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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,853 recalls have been announced year to date.
  • Oct 2026 was 45% lower than the previous complete period (Sep 2026: 209).
  • The highest complete period was Jun 2026 (300).
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,450
Class I9,860
Class III2,901
Not Yet Classified2

Showing 3,681–3,700 of 19,206 recalls

FDA Recall United States TerminatedTerminated: July 23, 2024Historical recordClass I

Newly Weds Foods, Inc.

Product
G96378 LOTTA ZING SAUCE MIX X2 15.00 CASE
Reason
Products may contain Salmonella
Published
July 12, 2023
Distribution
ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…

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FDA Recall United States TerminatedTerminated: July 23, 2024Historical recordClass I

Newly Weds Foods, Inc.

Product
A89471 BATTER MIX X1 50.00 BAG
Reason
Products may contain Salmonella
Published
July 12, 2023
Distribution
ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…

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FDA Recall United States TerminatedTerminated: July 23, 2024Historical recordClass I

Newly Weds Foods, Inc.

Product
A53643 BREADER X1 50.00 BAG
Reason
Products may contain Salmonella
Published
July 12, 2023
Distribution
ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…

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FDA Recall United States TerminatedTerminated: July 23, 2024Historical recordClass I

Newly Weds Foods, Inc.

Product
A21470 BATTER MIX X1 50.00 BAG
Reason
Products may contain Salmonella
Published
July 12, 2023
Distribution
ALABAMA, ARKANSAS, CALIFORNIA, COLORADO,…

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FDA Recall TerminatedTerminated: December 18, 2023Historical recordClass II

Amphotericin B Liposome for Injection, 50mg/vial, Rx only, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by Sun Pharmaceutical Medicare Limited, Baska Ujeti Road, Ujeti, Halol-389350, Gujarat, India, NDC 62756-0233-01

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason
Subpotent drug
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-112-01

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

StellaLife VEGA Oral Care Gel, 1 fl oz (30 ml) tubes, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-102-02

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

StellaLife VEGA Oral Care Spray, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-101-02

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Coconut, Distributed by: StellaLife, Aventura, FL NDC 69685-113-16

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

StellaLife VEGA Oral Care Rinse, 16 fl oz (473 ml) bottles, Peppermint, Distributed by: StellaLife, Inc., Aventura, FL NDC 69685-103-16

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

SnoreStop Naso Spray Bulk, liquid, Distributed by Green Pharma, NDC 61152-199-99

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

Babelyn Diarrhea Drops Homeopathic Remedy, 0.5 fl. oz. (15 mL) bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-035-01

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

Bebelyn Colic Drops Homeopathic Remedy, 0.5 FL Oz (15 mL) bottles, distributed by Pharmadel LLC Georgetown, DE NDC 55758-036-01

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical recordClass II

Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 16, 2024Historical 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

by Homeocare Laboratories, Inc.

Reason
cGMP deviations
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 5, 2024Historical 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

by Ferring Pharmaceuticals Inc

Reason
cGMP deviations: potential for Microbial Contamination of Non-Sterile Products
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall TerminatedTerminated: April 30, 2024Historical 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

by The Harvard Drug Group

Reason
Packaging defect: blister packaging inadequately sealed.
Published
July 5, 2023
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: April 9, 2024Historical recordClass II

Rudolph Foods Company

Product
Rudolphs OnYums Onion Flavored Snack Rings 3 oz. UPC 0-24…
Reason
Undeclared wheat and artificial colors (Yellow 6, Yellow Lake 6, Blue 2 Lake, Blue 1 Lake, Red 40 Lake)
Published
July 5, 2023
Distribution
Arkansas, Colorado, Illinois, Indiana, I…

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FDA Recall TerminatedTerminated: July 2, 2024Historical 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

by The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

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

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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.

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