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Recall totals

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

37,324

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 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

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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated October 21, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

USDA FSIS Recall United States Status not reported2026 record

Kayem Foods Inc. Recalls Meat and Poultry Products Due to Possible Temperature Abuse

Reason: <img align="left" hspace="5" src="https://www.fsis.usda.gov/sites/default/files/2023-04/Icon-Recalls.png"/> WASHINGTON, Oct. 17, 2026 - Kayem Foods Inc., a Chelsea, Mass. establishment, is recalling approximately 1,584,361 pounds of ready-to-eat (RTE) meat and poultry products because they may have experienced temperature...
Published: October 17, 2026

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FDA Recall United States Status not reported2026 record

Lidl US Recalls Gelatelli Coffee & Vanilla Gelato Due to Possible Health Risk

Reason: ARLINGTON, VA – OCTOBER 16, 2026 – Lidl US is recalling one lot of Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces 16 FL OZ (1 PT) UPC 4 0564897 22458 Lot: 085261 Best By MAR/26/2028 because it has the potential to be contaminated with Listeria monocytogenes, an organism which ca
Published: October 16, 2026

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FDA Recall United States Status not reported2026 record

Family Farmstead Dairy Announces Recall of Raw Mild Cheddar Cheese Due to Potential E. coli O26:H11 and O45:H2 Contamination

Reason: WORCESTER, NY, October 15, 2026 - Family Farmstead Dairy of Worcester, NY is recalling specific lot of cheddar cheese because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy ad
Published: October 15, 2026

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FDA Recall United States Status not reported2026 record

Family Farmstead Dairy Announces Recall of Raw Mild Cheddar Cheese Due to Potential E. coli O157:H7 Contamination

Reason: WORCESTER, NY, October 15, 2026 - Family Farmstead Dairy of Worcester, NY is recalling specific lot of cheddar cheese because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy ad
Published: October 15, 2026

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FDA Recall Ongoing2026 recordClass II

Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06.

by Apothecary Pharma LLC

Reason: Lack of Assurance of Sterility
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC 27513, NDC 85091-001-18.

by Apothecary Pharma LLC

Reason: Lack of Assurance of Sterility
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Tretinoin Cream UPS, 0.05%, 20g, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals USA Inc., Hawthorne, NY 10532, NDC 51672-1394-0.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Impurities/Degradation Specifications
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Tretinoin Cream USP, 0.05%, 45 g tube, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Product of Canada, NDC 16714-249-02.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Impurities/Degradation Specifications
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass III

Tretinoin Cream USP, 0.05%, 45g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals USA Inc., Hawthorne, NY 10532, NDC 51672-1394-9.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Impurities/Degradation Specifications
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/40, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

TIRZEPATIDE/CYANOCOBALAMIN 64/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

TIRZEPATIDE/CYANOCOBALAMIN 26/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/60, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

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FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS), 30/1/40, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

View recall →

FDA Recall Ongoing2026 recordClass II

Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,

by Carolina Infusion, LLC

Reason: Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
Published: October 14, 2026
Distribution: Nationwide

View recall →

Data last updated: October 21, 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.