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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

State: NY ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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 I

EATALY NY, LLC (DUTY ONLY)

Product: eataly artichoke spread, net wt. 7oz 200g, UPC 612067
Reason: Product contains undeclared walnuts.
Published: May 9, 2018
Distribution: NY

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FDA Recall United States Terminated Historical recordClass II

Riddhi USA Inc.

Product: All dietary supplements manufactured and distributed by Ridd…
Reason: Per order of the Consent Decree, firm is recalling all dietary supplements.
Published: May 9, 2018
Distribution: Multiple states

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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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Data last updated: September 30, 2026 ET

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.