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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: NH ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 13, 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 III

The Chai Box

Product: THE CHAI BOX CHAI CONCENTRATE UNSWEETENED 16FL OZ/473ML glas…
Reason: Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9.
Published: November 2, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass III

The Chai Box

Product: THE CHAI BOX CHAI CONCENTRATE 16FL OZ/473ML glass bottles UP…
Reason: Potential to be contaminated with Clostridium botulinum. Product was tested and found to have pH level of 4.9.
Published: November 2, 2022
Distribution: Product was shipped to the following sta…

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FDA Recall United States Terminated Historical recordClass II

Secrets Of The Tribe

Product: Indian Gooseberry Alcohol-Free Extract, 2 oz. glass bottle,…
Reason: Product has elevated level of lead.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Secrets Of The Tribe

Product: Amla Alcohol-Free Extract, 2 oz. glass bottle, UPC 041979376…
Reason: Product has elevated level of lead.
Published: November 2, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE, USP - 900 mg, WATER FOR INJECTION, USP - qs, 1000mL Bag, 12 PK, Rx Only, Fresenius Medical Care North America, Waltham, MA 02451, NDC 49230-300-10

by Fresenius Medical Care Holdings, Inc.

Reason: Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough ACETAMINOPHEN/ PAIN RELIEVER DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT GUAIFENESIN/ EXPECTORANT PHENYLEPHRINE HCl/ NASAL DECONGESTANT Maximum Strength Decongestant Free DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015 walgreens.com

by LNK International, Inc.

Reason: Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Acyclovir Sodium Injection, 500mg/10mL (50mg/mL), 10 mL Single Dose Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd., E. Windsor, NJ 08520; Made in India, NDC 55150-154-10.

by AuroMedics Pharma LLC

Reason: Presence of Particulate Matter: Customer complaint for a dark red, brown and black particulate floating inside vial.
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin Capsules, USP, 150 mg, 30-count bottle, Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA, NDC 51407-322-30

by Golden State Medical Supply Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Rifampin Capsules, USP, 300 mg, packaged in a) 30-count bottle (NDC 51407-323-30), b) 60-count bottle (NDC 51407-323-60), c) 100-count bottle (NDC 51407-323-01), Rx only, Manufactured by Patheon Pharmaceuticals Inc., OH, Packaged by GSMS, Incorporated, CA.

by Golden State Medical Supply Inc.

Reason: Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Published: October 26, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II