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

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Source: FDA and USDA public dataLast updated September 12, 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 Ongoing Historical recordClass II

Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42

by Denver Solutions, LLC DBA Leiters Health

Reason: Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 mL cases, Magnus 16005 Gateway Drive, Ste 300, Frisco, TX 75033

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 330 Gal. cases, Distributed by: Magnus, 16005 Gateway Drive, Suite 300, Frisco, TX 75033

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser, Benzalkonium Chloride 0.13% Antibacterial, a) 1250 mL cases, b) 1 G cases, mountain spring scent, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471.

by Seatex LLC

Reason: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains 40mg of omeprazole and 1,680mg of sodium bicarbonate, Directions for Use: Empty packet contents into a small cup containing 1 to 2 tablespoons of WATER. DO NOT USE OTHER LIQUIDS OR FOODS. Stir well and drink immediately. Rx Only, Distributed by: Oceanside Pharmaceuticals, a division of Bausch Health US, LLC, Bridgewater, NJ 08807, NDC 68682-991-30.

by Bausch Health Companies, Inc.

Reason: Subpotent Drug: Out of specification for assay
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Lubricant PM Ointment (Mineral Oil 42.5% and White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by: AACE Pharmaceuticals, Inc., Fairfield, NJ 07004, NDC 71406-124-35, UPC 371406124356

by Brassica Pharma Pvt Ltd

Reason: Lack of Assurance of Sterility
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

CVS Health Lubricant Eye Ointment (Mineral oil 31.9% Emollient, White petrolatum 57.7% Emollient), Packaged in in 3.5 gram tubes, Distributed by: CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, NDC 76168-707-35, UPC 050428634141

by Brassica Pharma Pvt Ltd

Reason: Lack of Assurance of Sterility
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Equate Stye Lubricant Eye Ointment (Mineral Oil 31.9%, White Petrolatum 57.7%), Packaged in 3.5 g tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-028-35, UPC 681131395304

by Brassica Pharma Pvt Ltd

Reason: Lack of Assurance of Sterility
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Equate Lubricant Eye Ointment (Mineral Oil 42.5%, White Petrolatum 57.3%), Packaged in 3.5 gram tubes, Distributed by Walmart Inc., Bentonville, AR 72716, NDC 79903-026-35, UPC 681131395298

by Brassica Pharma Pvt Ltd

Reason: Lack of Assurance of Sterility
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Mesalamine Extended-Release Capsules, USP 500mg, Rx Only, 120 Capsules per bottle, Manufactured by: Sun Pharmaceutical Industries Limited, Mohali, INDIA, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 63304-089-13.

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Failed Dissolution Specifications: Out of specification for dissolution.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill, Rx only, Manufactured by: Apotek Inc., Toronto, Ontario, Cananda, Marketed by: GSMS Incorporated, Camarillo, CA, NDC 60429-195-15

by Golden State Medical Supply Inc.

Reason: CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Ready Pac Foods Inc

Product: Ready Pac Bistro Fresh Mex Chopped Kit 10.5 oz. UPC 07774525…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: March 6, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

Ready Pac Foods Inc

Product: Marketside Bacon Ranch Crunch Kit 9.8 oz. UPC 681131305440
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: March 6, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

Ready Pac Foods Inc

Product: Ready Pac Bistro Queso Crunch Salad Kit 24 oz. UPC 077745256…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: March 6, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass I

Ready Pac Foods Inc

Product: Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: March 6, 2024
Distribution: U.S. distribution to the following: CA,…

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FDA Recall United States Terminated Historical recordClass II

Reser's Fine Foods, Inc.

Product: The recalled Reser's Amish Macaroni Salad was packaged in a…
Reason: Undeclared Wheat. The recalled Reser's Amish Macaroni Salad was packaged in a plastic container where the top lid is correctly labeled as Reser s Amish Macaroni Salad but the container side label mis-labeled as Reser s Southern Style with Egg Potato Salad. The ingredient statement on the Reser s Southern Style with Egg Potato Salad container side label does not declare wheat.
Published: March 6, 2024
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Clobazam Tablets 10mg, 100-count bottle, Rx Only, Manufactured by: Micro Labs Limited Goa-403 722, India. Manufactured for: Micro Labs USA, Inc. Somerset, NJ 08873. NDC 42571-315-01

by Micro Labs Limited

Reason: CGMP Deviations: Out of specification for residual solvents.
Published: February 28, 2024
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

CABTREO (clindamycin phosphate, adapalene and benzoyl peroxide) Topical Gel 1.2%/0.15%/3.1%, Not for Oral, Ophthalmic or Intravaginal Use, Rx Only, Net Wt. 50g, Distributed by Bausch Health US, LLC Bridgewater, NJ 08807 USA, Manufactured by: Bausch Health Companies, Inc. Laval Quebec H7L 448, Canada, NDC 0187-0006-25.

by MCKESSON CORPORATION

Reason: CGMP Deviations: Product was stored outside labeled storage temperature requirements. Product was exposed to controlled room temperature environment instead of remaining refrigerated.
Published: February 28, 2024
Distribution: Nationwide

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Data last updated: September 12, 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.