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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.

37,115
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,793
Class I recallsReasonable probability of serious health consequences
24,343
Class II recallsTemporary or medically reversible health consequences
2,887
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 2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 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)

  • 1,527 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
Recalls by class

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

Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,343
Class I9,793
Class III2,887
Not Yet Classified1

Showing 5,961–5,980 of 20,769 recalls

FDA Recall Completed Historical recordClass I

SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.

by Fagron, Inc

Reason
Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
Published
May 18, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, NDC 55513-0206-01

by Amgen, Inc.

Reason
Defective container: loose crimp defect, potential loss of container integrity.
Published
May 18, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer Inc, NY, NY 10017, NDC 0009-0068-07.

by Viatris Inc

Reason
Failed Dissolution Specifications: low out of specification results for dissolution.
Published
May 18, 2022
Distribution
Nationwide

View recall →

FDA Recall United States Terminated Historical recordClass III

Rong Shing Trading NY Inc

Product
'KORICA' ROASTED PEANUT; 10.6OZ (300G); packaged in plastic…
Reason
Product contains cyclamate, an unapproved color.
Published
May 18, 2022
Distribution
IL, IN, WA, NY, NJ, FL, MN, CT, MA, CA,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Sugar-Free Xylitol NET 8.45 FL OZ…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

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FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ (250…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Rock Sugar Flavor NET 4.45 FL OZ…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Honey Flavor NET 8.45 FL OZ (250m…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Coconut Flavor NET 8.45 FL OZ (25…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

View recall →

FDA Recall United States Terminated Historical recordClass II

Eastland Food Corporation

Product
Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250…
Reason
Deficient packaging material potentially leading to premature spoilage.
Published
May 18, 2022
Distribution
Retail stores in AL, CA, CO, CT, DE, FL,…

View recall →

FDA Recall Terminated Historical recordClass I

The Mandalorian Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./60 mL bottles, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-012-02

by Best Brands Consumer Products, Inc.

Reason
Chemical Contamination; FDA analysis found product to contain benzene
Published
May 11, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass I

Mickey Mouse Hand Sanitizer, ethyl alcohol 68%, 2.11 oz./to mL bottle, Best Brands Consumer Products, Inc., c/o Best Brands Sales Company LLC, New York, NY NDC 74530-013-02

by Best Brands Consumer Products, Inc.

Reason
Chemical Contamination; FDA analysis found product to contain methanol
Published
May 11, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Pantoprazole Sodium Delayed-Release Tablets, USP, 20 mg, Rx Only, 90 tablets per bottle, Manufactured by: Torrent Pharmaceuticals Ltd., Indrad-382 721, India, Manufactured for: Torrent Pharma Inc., Levittown, PA 19057, NDC# 13668-096-90.

by Torrent Pharma Inc

Reason
CGMP deviations: tablets cracking
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Erythromycin Topical Gel USP, 2%, Net Wt 60 g tube, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-053-68

by McKesson Corporation dba McKesson Drug Company

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented) (Potency expressed as betamethasone), 15 gram tube, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-996-65

by McKesson Corporation dba McKesson Drug Company

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Lidocaine Prilocaine Cream USP, 2.5%/2.5% Net Wt. 30 gram tube, Rx Only, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southridge Blvd., Suite 101 Memphis, TN 38141 Manufactured by: Teligent Pharma, Inc., Buena, NJ 08310, NDC 63739-054-66

by McKesson Corporation dba McKesson Drug Company

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL), 50 mL bottle, Rx only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310 Distributed by: McKesson Corporation dba Sky Packaging 4071 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-977-64

by McKesson Corporation dba McKesson Drug Company

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Halobetasol Propionate Ointment 0.05% Net Wt., 50 gram tube, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging 4071 Southridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-998-67

by McKesson Corporation dba McKesson Drug Company

Reason
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100 mL per bottle, Rx only, Manufactured by Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701, NDC 50383-775-04

by Akorn, Inc.

Reason
Failed viscosity specification - product was below specificcation
Published
May 11, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.

by Viatris Inc

Reason
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Published
May 11, 2022
Distribution
Nationwide

View recall →

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.