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Recall totals

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

37,450

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresh-ready-foods-llc-recalls-fresh-you-brand-sausage-egg-cheese-biscuit-sandwich-due-possiblePublished November 8, 2026

Most affected stateHawaii 200 recalls mention this state

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated November 9, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Standard Starter TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

TPN Neonatal all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Ropi/ Epi/ Clon PeriCapsular injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

NOVA PeriCapsular injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

RECK PeriCapsular injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Nalbuphine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Lidocaine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Ropivacaine HCl in 0.9% Sodium Chloride all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 18, 2017Historical recordClass II

Bupivacaine HCl in 0.9% Sodium Chloride all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054

by Advanced Pharma Inc.

Reason: Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 1, 2019Historical recordClass II

Estrone, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-0445-1), b) 5 G bottle (NDC 51552-0445-2), c) 25 G bottle (NDC: 51552-0445-4), d) 100 G bottle (NDC: 51552-0445-5), RX only, Distributed by Fagron, Inc. 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel. 1-(800) 423-6967 Also packaged as: Estrone USP, For Prescription Compounding, packaged in a) 1 G bottle (NDC 52372-9494-01), b) 5 G bottle (NDC 52372-9494-05), c) 25 G bottle (NDC 52372-9494-03), d) 100 G bottle ( NDC 52372-9494-02), Rx only, Distributed by FREEDOM 801 W. New Orleans St. Broken Arrow, OK 74011 Tel. (877) 839-8547

by Fagron, Inc

Reason: cGMP Deviations: lack of quality assurance at the API manufacturer.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 1, 2019Historical recordClass II

Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3), d) 100 G bottle (NDC: 51552-1392-5), RX only, Distributed by Fagron, Inc. 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel. 1-(800) 423-6967 Also packaged as: Estriol USP Micronized, For prescription compounding, packaged in a 100 G bottle (NDC 52372-9292-01), Rx only, Distributed by FREEDOM, 801 W. New Orleans St. Broken Arrow, OK 74011

by Fagron, Inc

Reason: cGMP Deviations: lack of quality assurance at the API manufacturer.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 12, 2017Historical recordClass II

Alprazolam Extended-release Tablets, USP, 1 mg, 60-count bottle, Rx Only, Manufactured and Distributed by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5022-91

by Mylan Pharmaceuticals Inc.

Reason: Failed Dissolution Specifications
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 27, 2019Historical recordClass I

HVF Inc. d.b.a Huson Valley Farms

Product: Nutty INFUSIONS Ginger Wasabi Cashew Butter, NET WT. 10 OZ (…
Reason: Listeria monocytogenes contamination
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 27, 2019Historical recordClass I

HVF Inc. d.b.a Huson Valley Farms

Product: Nutty INFUSIONS Roasted Cashew Butter, NET WT. 10 OZ (284 g)
Reason: Listeria monocytogenes contamination
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 20, 2018Historical recordClass III

RB Manufacturing LLC

Product: Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosa…
Reason: RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Published: May 31, 2017
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: June 14, 2017Historical recordClass I

U S Deer Antlers Export & Import

Product: Herbal Tea Variety 120 ml/pouch, 40 pouches/case
Reason: US Deer Antler Export and Import is recalling a variety of Herbal Teas because they may be contaminated with Clostridium botulinum
Published: May 31, 2017
Distribution: US: CA, TX, NC, NY, VA, HI, GA, WA, IL,…

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FDA Recall United States TerminatedTerminated: July 7, 2017Historical recordClass I

Italian Gluten Free Foods CL

Product: Chef Luca's Italian Gluten Free Foods Lasagna Al Forno Baked…
Reason: Product contains undeclared eggs
Published: May 31, 2017
Distribution: MA, CT, NY, NJ, VA, DE, MD, P A, TX

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FDA Recall United States TerminatedTerminated: January 14, 2021Historical recordClass II

Rich Products Corp

Product: ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 0…
Reason: The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Published: May 31, 2017
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 14, 2021Historical recordClass II

Rich Products Corp

Product: 7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 12…
Reason: The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Published: May 31, 2017
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 14, 2021Historical recordClass II

Rich Products Corp

Product: ARTISAN-STYLE PIZZA DOUGH BALL distributed under the followi…
Reason: The product was made with flour supplied by Ardent Mills who issued a recall on flour products due to possible E. coli 0121 contamination.
Published: May 31, 2017
Distribution: Multiple states

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Data last updated: November 9, 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.