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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 6,801–6,820 of 22,138 recalls

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403. NDC: 11673-759-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, MADE WITH PRIDE & CARE FOR H-E-B SAN ANTONIO, TX 78204. NDC: 37808-759-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by: Walmart, Inc., Bentonville, AR 72716. NDC: 49035-042-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Target Corp., Minneapolis, MN 55403 NDC: 11673-130-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY DOLGENCORP, LLC, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072. NDC: 55910-251-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716. NDC: 49035-959-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-818-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed By Perrigo, Allegan, MI 49010. NDC: 0113-8959-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202. NDC: 30142-818-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Infant's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC: 59779-946-16

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403. NDC: 11673-133-16

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC: 0363-0971-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Cherry Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 45802-203-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1321-97

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Children's Pain & Fever Bubblegum Flavored Acetaminophen Suspension (160mg/5ml), 4 fl oz (118 mL) per bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716. NDC: 49035-313-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass II

Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 50941-009-43

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Azacitidine, 100mg/vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-465-62

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Terminated Historical recordClass III

Azacitidine, 1,00mg/Vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-305-62

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Published
March 2, 2022
Distribution
Nationwide

View recall →

FDA Recall Ongoing Historical recordClass II

Methylphenidate Hydrochloride Chewable Tablets, 2.5 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharmaceuticals Inc., Saddle Brook, NJ 07863, NDC 64980-221-01

by RISING PHARMACEUTICALS

Reason
Failed Tablet Specifications: Recall of this drug product was voluntarily initiated by the manufacturer due to a market complaint, which stated that a tablet in the sealed bottle was twice larger in size when compared to the remaining tablets. This complaint is second of its kind.
Published
March 2, 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.