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Recall totals

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

37,142

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

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 recallhttps://www.fsis.usda.gov/recalls-alerts/fontanini-foods-llc-recalls-raw-frozen-pork-sausage-products-due-possible-foreignPublished September 25, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 26, 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	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall United States Terminated Historical recordClass I

Pacific Coast Fruit Company

Product: Carnival Cauli Florets, 6/16 oz., RETAIL item # 73633, New…
Reason: Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.
Published: November 8, 2017
Distribution: distributed in Oregon and Washington.

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Veggie Pack with Dressing, Alaska Carrot brand, 12 x 12 oz.…
Reason: Veggie products product are recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Stir Fry Kit, Alaska Carrot, 1 x 11 lb. per case, UPC 45009…
Reason: Stir Fry Kit product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Broccoli Crunch Kit, Alaska Carrot brand, 1 x 6 lb. per cas…
Reason: Broccoli Crunch Kit product is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass I

Triple B Corporation

Product: Salad Kit, Super Slaw CPF, Produced by CP Fresh of Seattle,…
Reason: Salad Kit, Super Slaw CPF is recalled due to possible contamination with Listeria monocytogenes. The broccoli used in processing this item has been recalled by vendor Mann Packing of Salinas, California.
Published: November 8, 2017
Distribution: distributed in Alaska, Idaho, Montana, O…

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FDA Recall United States Terminated Historical recordClass II

Midway Specialty Vehicles LLC

Product: Oatmeal Cookie, 60-2.5 oz. cookies, frozen
Reason: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain traces of undeclared peanut or tree-nut allergens.
Published: November 8, 2017
Distribution: Domestic Only: MI, IN, IL, OH, NJ, WA, C…

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FDA Recall United States Terminated Historical recordClass II

Midway Specialty Vehicles LLC

Product: M&M Cookie, 60- 2.5 oz. cookies, frozen
Reason: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain traces of undeclared peanut or tree-nut allergens.
Published: November 8, 2017
Distribution: Domestic Only: MI, IN, IL, OH, NJ, WA, C…

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FDA Recall United States Terminated Historical recordClass II

Midway Specialty Vehicles LLC

Product: Triple Chocolate Mudslide Cookie, 120 1 oz. cookies, frozen
Reason: Midway Specialty Vehicles, LLC dba Aunt Beths Cookies, is voluntarily recalling multiple varieties of cookies sold between January 1, 2017 and September 28, 2017, because they may contain traces of undeclared peanut or tree-nut allergens.
Published: November 8, 2017
Distribution: Domestic Only: MI, IN, IL, OH, NJ, WA, C…

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FDA Recall United States Terminated Historical recordClass I

Pacific Coast Fruit Company

Product: Kit Cauliflower Tabouleh, 2/4.5 lbs., Food Service item # 71…
Reason: Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.
Published: November 8, 2017
Distribution: distributed in Oregon and Washington.

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FDA Recall United States Terminated Historical recordClass I

Pacific Coast Fruit Company

Product: Kit Cauliflower Cake FK, 6.6 lbs, Food Service item # 73706,…
Reason: Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.
Published: November 8, 2017
Distribution: distributed in Oregon and Washington.

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FDA Recall United States Terminated Historical recordClass I

Pacific Coast Fruit Company

Product: Vegetable Tray, 2/25 oz., RETAIL item # 71444, Pacific Coast…
Reason: Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes. The firm utilized a portion of the salads that were recalled by their supplier.
Published: November 8, 2017
Distribution: distributed in Oregon and Washington.

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FDA Recall Terminated Historical recordClass III

Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716, NDC # 4903594126 UPC # 681131150774. Studio 35 Beauty Daily Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed By: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, NDC # 0363001726, UPC # 049022889125

by Vi-Jon, Inc.

Reason: Failed Stability Specifications
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 0591-5884-01.

by Teva Pharmaceuticals USA

Reason: Failed Dissolution Specifications: Low out of specification results for dissolution.
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India, Distributed by: Wockhardt, USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054, USA. NDC: 64679-924-03;

by Wockhardt Usa Inc.

Reason: Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-243-03

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx Only , Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-245-02

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130, Sugar Land, TX 77478, NDC# 71019-243-01

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's USP in 500 mL bag, Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-242-01

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-05.

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection USP in 1000 mL bag Rx Only, Compounded by PharMEDium Services, LLC. 12620 W. Airport Blvd. #130 Sugar Land, TX 77478, NDC# 71019-241-04

by PharMEDium Services, LLC

Reason: Subpotent Drug
Published: November 1, 2017
Distribution: Nationwide

View recall →

Data last updated: September 26, 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.