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Recall totals

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

37,449

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 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 7, 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 United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 4-12-14-18-23-25-AA from Pr…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 2-3-6-8-10-14-16-22-23-24 f…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 4-6-9-10-11-13-15-20 from P…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 1-2-3-5-9-11-15-17-19-25 fr…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 2-4-5-8-15-19-20-22-24-AA f…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 2-3-8-10-15-18-19-22-23 fro…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 2-5-8-9-16-19-21-22-23-24-2…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: September 1, 2022Historical recordClass I

HELLOFRESH US

Product: HelloFresh Meal Kit Product Code 2-7-17-19-21-25-AB from Pro…
Reason: Products contain onions purchased from ProSource and associated with a Salmonella Oranienburg outbreak.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: February 8, 2022Historical recordClass I

JF Palmer & Sons Produce

Product: Onions Red Jumbo, packaged in 25 pound bulk bags
Reason: Potential to be contaminated with Salmonella
Published: November 24, 2021
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: February 8, 2022Historical recordClass I

JF Palmer & Sons Produce

Product: Onions White, Medium, Large, Jumbo, packaged in 50 pound bu…
Reason: Potential to be contaminated with Salmonella
Published: November 24, 2021
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: February 8, 2022Historical recordClass I

JF Palmer & Sons Produce

Product: Onions Yellow, Small, Medium, Large, Jumbo, Colossal, Super…
Reason: Potential to be contaminated with Salmonella
Published: November 24, 2021
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: March 2, 2023Historical recordClass I

Greenhead Lobster Products LLC

Product: Greenhead Lobster brand Frozen Cooked Claw and Knuckle Meat…
Reason: Products may be contaminated with Listeria monocytogenes.
Published: November 24, 2021
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: August 2, 2022Historical recordClass I

KEELER FAMILY FARMS

Product: Whole raw onions - YELLOW - imported from Chihuahua, Mexico…
Reason: Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 2, 2022Historical recordClass I

KEELER FAMILY FARMS

Product: Whole raw onions - WHITE - imported from Chihuahua, Mexico a…
Reason: Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: August 2, 2022Historical recordClass I

KEELER FAMILY FARMS

Product: Whole raw onions - RED - imported from Chihuahua, Mexico and…
Reason: Potential contamination with Salmonella Oranienburg in onions from Chihuahua, Mexico.
Published: November 24, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 1, 2022Historical recordClass II

Tadalafil Tablets, USP 20 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-077-01

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Published: November 17, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: September 1, 2022Historical recordClass II

Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-075-01

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Published: November 17, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 14, 2024Historical recordClass II

Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 30-count case: 68094-330-62), and b) 100-count case (NDC 100-count case: 68094-330-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: cGMP Deviations: Product manufactured with contaminated raw ingredient.
Published: November 17, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: July 14, 2024Historical recordClass II

Acetaminophen Oral Suspension, 160 mg/5 mL, packaged in 5 mL per cup (NDC Individual cup: 68094-231-59), in a) 30-count case (NDC 30-count case: 68094-231-62), and b) 100-count case (NDC 100-count case: 68094-231-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: cGMP Deviations: Product manufactured with contaminated raw ingredient.
Published: November 17, 2021
Distribution: Nationwide

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FDA Recall TerminatedTerminated: December 21, 2022Historical recordClass II

Cefixime Capsules 400 mg, 50 capsules bottles, Rx Only, Manufactured by: Alken Laboratories Ltd., Mumbai - 400 013, India, Distributed by: Ascend Laboratories LLC, Parsippany, NJ, 07054 NDC 67877-584-50

by Ascend Laboratories LLC

Reason: Failed Impurities/Degradation Specifications
Published: November 17, 2021
Distribution: Nationwide

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Data last updated: November 7, 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.