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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 14, 2026 ET

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

Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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 Terminated Historical 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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FDA Recall United States Terminated Historical recordClass I

Simply Delicious, Inc.

Product: Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack,…
Reason: Almond Butter Bars contain undeclared peanuts.
Published: November 17, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial, Rx only. Manuf. for: Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, USA. Manuf. by: Baxter Pharmaceuticals LLC., Bloomington, IN 47403, USA, NDC: 67919-011-01

by MERCK SHARP & DOHME CORP

Reason: Presence of Particulate Matter: Identified as Glass Particles
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Reason: Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 count (NDC 68180-414-06) and b) 90 count (NDC 68180-414-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published: November 10, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 count (NDC 68180-413-06) and b) 90 count (NDC 68180-413-09) bottles, Rx only

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Published: November 10, 2021
Distribution: Nationwide

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Data last updated: September 14, 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.