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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: SC ×
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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 Terminated Historical recordClass II

HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in 0.9% Sodium Chloride 50 mL (HYDROmorphone Total Dose 1000 mcg) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0331-22

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

HYDROmorphone HCL 1 mg per mL in 0.9% Sodium Chloride 25 mL Fill in 30 mL single-dose syringe (Total Dose Hydromorphone 25 mg/25 mL) Rx Only SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0303-17

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SUCcinylcholine 20 mg per mL, Total Volume 10 mL in single-dose syringe, (SUCcinylcholine 200 mg / 10 ml) Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR NDC 70004-0910-29

by SCA Pharmaceuticals, LLC

Reason: Lack Of Assurance Of Sterility.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

A1 Slim, Dietary Supplement Beautifully Slim, capsule, 350 mg, 30-count bottle, A1 Slim LLC Pearland TX 77584, www.A1SLIM.COM, info@a1slim.com Bar-Code A105212014

by Kiriko, LLC.

Reason: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sibutramine, phenolphthalein, and n-desmethyl sibutramine, making this an unapproved drug for which safety and efficacy have not been established and therefore, subject to recall.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.

by Precision Dose Inc.

Reason: Subpotent Drug: low out of specification results.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Clofarabine injection, 20 mg/20 mL, 20 mL Single-Use Vial, Rx only, Mfd by: Teva Pharmachemle, Swensweg 5, Haarlem, The Netherlands; Mfd for: Winthrop U.S., a business of sanofi-aventis U.S. LLC, Bridgewater, NJ 08807; NDC 0955-1746-01.

by Sanofi-Aventis U.S. LLC

Reason: Labeling: Incorrect or Missing Package Insert: authorized generic product was packaged with the incorrect insert for the brand name product Clolar (clofarabine) injection.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.

by AVKARE Inc.

Reason: Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Earthbound Farm, LLC

Product: Earthbound Farm¿ Organic Chopped Asian Style Salad Kit; 11 o…
Reason: Recall of Asian Style Chopped Salad Kit because in some instances the dressing and toppings packets inside the bag are not those foe the salad. Some of the Asian Style Salad Kits could have the dressing packet for the Southwest Chopped Salad Kit which contains egg and milk that are not declared as ingredients on the bag of the Asian Style Salad Kit.
Published: November 8, 2017
Distribution: Alaska, Arizona, California, Colorado, F…

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FDA Recall United States Terminated Historical recordClass II

Midway Specialty Vehicles LLC

Product: Snickerdoodle 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: Frosted Brownie Cookie, 96 1.5 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: Red Velvet 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: Iced Sugar Frosted 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: Chocolate Chip-N-Chunk Cookie, 72- 2 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: Amish Sugar Cookie, 96- 1.5 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 I

Tres Latin Foods

Product: Tres Latin Foods Pupusas, Stuffed Corn Tortillas with Black…
Reason: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Published: November 8, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Tres Latin Foods

Product: Tres Latin Foods Kale & Pinto Bean pupusas Stuffed Corn Tort…
Reason: Tres Latin Foods is recalling specific code dates of Kale & Pinto Bean 10 oz. Pupusas and Black Bean and Sweet Corn 10 oz. Pupusas due to undeclared milk allergen.
Published: November 8, 2017
Distribution: Nationwide

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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 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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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.