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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 October 2026.

37,271
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,852
Class I recallsReasonable probability of serious health consequences
24,397
Class II recallsTemporary or medically reversible health consequences
2,897
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 2,085 recalls
Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 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)

  • 1,739 recalls have been announced year to date.
  • Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
  • The highest complete period was Jun 2026 (300).
  • Oct 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 II24,397
Class I9,852
Class III2,897
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,397
Class I9,852
Class III2,897
Not Yet Classified2

Showing 2,721–2,740 of 21,188 recalls

FDA Recall OngoingHistorical recordClass II

Moxifloxacin 4 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-511-08

by Imprimis NJOF, LLC

Reason
Lack of Assurance of Sterility
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Moxifloxacin 0.8 mg/0.8 mL Preservative-Free 0.8mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-509-08

by Imprimis NJOF, LLC

Reason
Lack of Assurance of Sterility
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Dexamethasone-Moxifloxacin- Ketorolac (1mg/mL, 0.5 mg/mL and 0.4 mg/mL), Preservative-Free, 1mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-513-01

by Imprimis NJOF, LLC

Reason
Lack of Assurance of Sterility
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Dexamethasone-Moxifloxacin (1 mg/mL and 5mg/mL) Preservative-Free, 1mL Single-Use vials for Intraocular Injection, Rx only, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-512-01

by Imprimis NJOF, LLC

Reason
Lack of Assurance of Sterility
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass II

Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free 1mL Single-Use vials for Intraocular Injection, Imprimis NJOF, LLC. 1705 Route 46 West, unit 6B, Ledgewood, NJ 07852, NDC 71384-640-01

by Imprimis NJOF, LLC

Reason
Lack of Assurance of Sterility
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall OngoingHistorical recordClass I

Tirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded Product By: Revive RX Pharmacy, 3831 Golf Dr A, Houston, TX 77018, internally assigned NDC 99000-9278-64

by Revive Rx LLC dba Revive Rx Pharmacy

Reason
Labeling: Label Mix-up - product labeled as tirzepatide contains testosterone cypionate
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall OngoingHistorical recordClass II

Zoledronic Acid Injection 5mg/100mL Sterile Solution, 100mL Single-Dose vials, Rx only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-688-52

by Dr. Reddy's Laboratories, Inc.

Reason
Lack of Assurance of Sterility: Leaking vials
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall TerminatedTerminated: August 11, 2025Historical recordClass II

Cathflo activase (ALTEPLASE), 2mg vials, Rx only, Genentech Inc., South San Francisco, CA 94080, NDC 50242-041-64

by Genentech, Inc.

Reason
Lack of Assurance of Sterility: Deformed stoppers observed during filling operations for Cathflo Activase.
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass II

Nutrition Corp

Product
Fresh N Lean brand Crustless Chicken Potato Pot Pie. Package…
Reason
Possible contamination with Listeria monocytogenes
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall United States OngoingHistorical recordClass I

Gibson Farms Inc

Product
Gibson Farms Organic Nuts -Light Halves and Pieces
Reason
Potential E. coli O157:H7 contamination.
Published
June 5, 2024
Distribution
U.S. distribution to the following: CA a…

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FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
9. 25pc Mother s Day heart ganache box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
8. 16pc Mother s Day ganache box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
7. 7pc Mother s Day heart box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

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FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
6. Mother s Day love purse
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
5. 9pc signature box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
4. 6pc signature ganache box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
3. 4pc ganache box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
2. 2pc signature Ganache box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall United States TerminatedTerminated: February 21, 2025Historical recordClass II

Maribel's Sweets, Inc.

Product
1. 2pc Ganache tote box
Reason
Contains undeclared coconut.
Published
June 5, 2024
Distribution
Nationwide

View recall →

FDA Recall CompletedHistorical recordClass I

Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton, NJ 08810, NDC 63037-123-25

by Hikma Injectables USA Inc

Reason
Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
Published
May 29, 2024
Distribution
Multiple states

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.

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