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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.

37,142
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,799
Class I recallsReasonable probability of serious health consequences
24,349
Class II recallsTemporary or medically reversible health consequences
2,891
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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 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 II24,349
Class I9,799
Class III2,891
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,349
Class I9,799
Class III2,891
Not Yet Classified1

Showing 11,941–11,960 of 20,239 recalls

FDA Recall United States Ongoing Historical recordClass I

Mccall Farms Inc

Product
Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredie…
Reason
Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach.
Published
May 9, 2018
Distribution
Florida, Georgia, Iowa, Illinois, Indian…

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FDA Recall United States Terminated Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the…
Reason
Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Viable Solutions, LLC

Product
Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the br…
Reason
Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass II

purely elizabeth.

Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz,…
Reason
Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Published
May 9, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

PYRIDOXINE Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

METHYLCOBALAMIN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIPO-PLEX Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIPO-DEN PLUS Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIPO-DEN EXTREME Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROXOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

ADENO-PLEX Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532

by Coastal Meds, LLC.

Reason
Presence of Particulate matter. Recall due to presence of unknown particulate matter.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Diltiazem HCl Extended-Release Capsules, USP 240 mg, 100-count bottles, Rx Only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-016-10

by Mckesson Packaging Services

Reason
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Diltiazem CD (Diltiazem Hydrochloride Extended-Release Capsules, USP) 180 mg, 100-count bottles, Rx Only Mfg. By: Actavis 60 Columbia Rd., Bldg. B Morristown, NJ 07960. NDC 63739-284-10

by Mckesson Packaging Services

Reason
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass III

Diltiazem HCl Extended-Release Capsules, USP 120 mg, 100-count bottles, Rx only, Mfg. By: Par Pharmaceutical One Ram Ridge Rd Chestnut Ridge, NY 10977. NDC: 63739-014-10

by Mckesson Packaging Services

Reason
Failed Dissolution Specifications. High dissolution results were obtained during stability testing.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Syringe. Premier Pharmacy Labs. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-234-14.

by Premier Pharmacy Labs Inc

Reason
Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Sterile Single-Dose Syringe. 8265 Commercial Way Weeki Wachee, FL 34613 NDC 69623-249-10

by Premier Pharmacy Labs Inc

Reason
Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.
Published
May 2, 2018
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a 3ml Sterile Single-Dose Syringe. 8265 Commerical Way Weeki Wachee, FL 34613. NDC 69623-127-10

by Premier Pharmacy Labs Inc

Reason
Lack of Assurance of Sterility:Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.
Published
May 2, 2018
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.