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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.

37,060
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/freshpoint-issues-recall-due-improperly-declared-allergen-egg-chicken-salad-wedge-sandwichesPublished September 8, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

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

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2
Download CSV
Recalls by class
ClassRecalls
Class II24,313
Class I9,786
Class III2,876
Not Yet Classified2

Showing 921–940 of 19,337 recalls

FDA Recall United States Terminated Historical recordClass II

Ventura Foods Llc

Product
Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 0051…
Reason
foreign objects (black plastic planting material) in granulated onion
Published
December 10, 2025
Distribution
The firm distributed product to 7 retail…

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product
Lava Bun with Salted Egg Yolk orange packaging (Frozen) U…
Reason
Products do not declare milk in the Contains statement or the ingredient statement.
Published
December 10, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Prime Food Processing LLC.

Product
Lava Bun with Green Tea Flavor bright lime green packaging…
Reason
Products do not declare milk in the Contains statement or the ingredient statement.
Published
December 10, 2025
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Costco Wholesale Corporation

Product
Costco Item# 11444 Kirkland Signature Chicken Sandwich with…
Reason
The 3oz. sealed packet of Caesar Dressing in Costco Chicken Sandwich w/ Caesar Salad may contain plastic material.
Published
December 10, 2025
Distribution
Item# 11444 Chicken Sandwich with Caesar…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Good & Gather Mozzarella & Parmesan shredded cheese blend, F…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Mozzarella and provolone shredded cheese blend (containing l…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Pizza style shredded cheese blend (containing low-moisture p…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Italian style shredded cheese blend (containing low-moisture…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Happy Farms by Aldi Italian Style shredded cheese blend (con…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Great Lakes Cheese Co Inc

Product
Low-moisture part-skim mozzarella shredded cheese, individua…
Reason
Potential metal fragments from supplier raw material (downstream recall)
Published
December 10, 2025
Distribution
AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN,…

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FDA Recall United States Terminated Historical recordClass II

Water Pure, Inc.

Product
My Bladder; Supports normal bladder tone & control; Dietary…
Reason
Product may be contaminated with E. coli O7:K1 (IAI39/ExPEC) and E. coli 1303
Published
December 10, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL vials, Rx only, Fresenius Kabi USA, LLC, NDC 63323-739-11 (unit of use), 63323-739-12 (unit of sale).

by Fresenius Kabi USA, LLC

Reason
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Published
December 3, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01

by Medical Products Laboratories, Inc.

Reason
Microbial contamination of a non-sterile product - microorganism found to be pseudomonas lactis
Published
December 3, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7074-26

by Otsuka ICU Medical LLC

Reason
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass I

POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC# 0990-7077-14

by Otsuka ICU Medical LLC

Reason
Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), and c) 800 mL (NDC 61924-405-27), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-435-04

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

by DermaRite Industries, LLC

Reason
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Published
November 26, 2025
Distribution
Nationwide

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Data last updated:

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.