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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

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

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Source: FDA and USDA public dataLast updated September 9, 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 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 Ongoing Historical recordClass III

Avion Pharmaceuticals, LLC

Product: Prenate Chewable¿ A chewable Rx prenatal vitamin with a deli…
Reason: Undeclared Soy. The firm received positive test results for soy which is not listed on the label. The firm also noticed that the amount of boron in the product is listed as 250mg per serving instead of 250mcg per serving.
Published: December 10, 2025
Distribution: Product was shipped to the following sta…

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FDA Recall United States Ongoing Historical recordClass II

Nutrition for Longevity

Product: Loaded Veggie Grain Bowl; NET WT. 10/90 OZ (309g) NO UPC Ide…
Reason: Potential contamination with Listeria monocytogenes.
Published: December 10, 2025
Distribution: Product was shipped directly to consumer…

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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 Completed Historical recordClass II

Dreyer's Grand Ice Cream, Inc.

Product: Retail Box: Haagen-Dazs mini chocolate dark chocolate ice cr…
Reason: Undeclared wheat.
Published: December 10, 2025
Distribution: U.S. Distribution: CA, KY, OH, WI

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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

Blonde Beard's

Product: Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce c…
Reason: Undeclared Soy
Published: December 10, 2025
Distribution: Product was distributed to Canada and th…

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FDA Recall United States Terminated Historical recordClass I

Africa Imports

Product: Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 K…
Reason: Product tested positive for Salmonella.
Published: December 10, 2025
Distribution: The adulterated product was sold to the…

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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 United States Ongoing Historical recordClass II

Nats Nuts LLC

Product: Nat's Nuts Cinnamon Whiskey Pecans, 4 oz.
Reason: Contains undeclared cashews
Published: December 3, 2025
Distribution: Connecticut, New York, New Jersey, and N…

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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: September 9, 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.