Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 16, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass II

Sodium Chloride 0.9%, USP, 1000 mL, Mfg by: Fresenius Medical Care North America, Waltham, MA 02451, NDC 46163-0300-10

by Fresenius Medical Care Holdings, Inc.

Reason: Temperature Abuse: Product exposed to temperature outside specified limits.
Published: June 16, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Arizona Nutritional Supplements

Product: 365 Everyday Value Whey Protein Powder Natural Vanilla Flavo…
Reason: Whey Protein Powder was mistakenly packaged with Soy Protein Powder.
Published: June 16, 2021
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

The Kroger Co

Product: Chicken Street Taco kit in a plastic tray with a clear plast…
Reason: Undeclared egg allergen for Chipotle Crema on product label.
Published: June 16, 2021
Distribution: Distributed to UT, NM, NV, AZ, WY, MT, I…

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FDA Recall United States Terminated Historical recordClass II

The Coca-Cola Company

Product: Glaceau Vitaminwater XXX labeled to be Glaceau Vitaminwater…
Reason: Product labeled to be "zero sugar" may contain sugar due to an incorrect label being used.
Published: June 16, 2021
Distribution: Distributed to distributors in AL, AR, C…

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FDA Recall United States Terminated Historical recordClass I

Gilster-Mary Lee Corp.

Product: Organic Microwave Butter Popcorn in cartons labeled to be Or…
Reason: Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk
Published: June 16, 2021
Distribution: Distributed to distribution centers in A…

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FDA Recall Terminated Historical recordClass I

1% Lidocaine HCl Injection, USP, 300 mg/30 mL (10 mg/mL), 30 mL Single-dose vial (NDC 0409-4279-16), packaged in 25 vials per tray (NDC 0409-4279-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published: June 9, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC 0409-1162-19), packaged in 25 vials per tray (NDC 0409-1162-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.

by PFIZER, INC

Reason: Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Published: June 9, 2021
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

BusPIRone Hydrochloride Tablets, USP, 15 mg, 100-count bottle, Rx only, Manufactured By: Oxford Pharmaceuticals, LLC Birmingham, Alabama 35211, NDC 69584-093-10

by Oxford Pharmaceuticals, LLC

Reason: Presence of Foreign Tablets/Capsules
Published: June 9, 2021
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III