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Recall totals

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

37,204

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,841

Class I recallsReasonable probability of serious health consequences

24,366

Class II recallsTemporary or medically reversible health consequences

2,892

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 2,073 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sierra-nevada-cheese-company-recalls-graziers-raw-milk-cheese-because-possible-health-riskPublished September 28, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 30, 2026 ET

Summary (Year to date)

1,714 recalls have been announced year to date.
Sep 2026 was 3% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (297).

Recalls by class

Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,366
Class I	9,841
Class III	2,892
Not Yet Classified	2

FDA Recall Terminated Historical recordClass II

Levophed norepinephrine bitartrate, injection, USP, 4 mg /4 mL (1 mg/mL),Rx only, Hospira, Inc. Lake Forest, IL --- NDC 0409-3375-04

by Hospira Inc., A Pfizer Company

Reason: GMP Deviation; A foreign stopper was observed during packaging of a lot of product.
Published: June 21, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

General Mills, Inc

Product: Chocolate chip cookie dough larabars, 10 count , UPC 100-219…
Reason: Chocolate chip cookie dough larabars which contain cashews were incorrectly packaged in peanut butter cookie larabars boxes. The individual labeling on the chocolate chip cookie dough larabars is correct despite being in the wrong boxes.
Published: June 21, 2017
Distribution: MN, WI AL, AZ, CA, CO, GA, IA,IN, KS,…

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FDA Recall Terminated Historical recordClass III

Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-778-01

by Hetero USA Inc

Reason: Presence of Foreign Substance: human hair melded into tablet.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 10 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only , For Subcutaneous Use Only Rx Only Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-010-01

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 12.5 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-012-01

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 15 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles. Sterile Office Use Only, For Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013, NDC: 69761-015-01

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 18 mg pellet , 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-018-01.

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 20 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count and 12 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-020-01

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 22 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-022-01

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol 25 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only. Rx Only ,Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-025-01,

by Qualgen

Reason: CGMP deviations- Lack of Quality Assurance
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010. NDC 0113-2003-12

by L. Perrigo Company

Reason: Defective Container: Carton is missing the tablet blister strip and tablet.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 40 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-137-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 30 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-113-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 20 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Zenatane (isotretinoin) Capsules, USP, 10 mg, 30-count (3 x 10 Prescription Packs) per carton, Rx Only, Manufactured By: Cipla Limited, Kurkumbh Village, Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Dissolution Specifications: out of specification results observed for low dissolution.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levonorgestrel, U.S.P. active pharmaceutical ingredient, packaged in 1 kg container, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code L1229.

by Spectrum Laboratory Products, Inc.

Reason: CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Estradiol (17-B-Estradiol; Estra-1,3,5(10)-triene-3, 17B-diol; Oestradiol) Plant Base, Micronized, U.S.P active pharmaceutical ingredient, packaged in 1g, 5g, 25g, 6 x 25g, and 100g containers, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901, Product code E1435.

by Spectrum Laboratory Products, Inc.

Reason: CGMP Deviations: these repackaged and redistributed products are being recalled due to a recall notice from the active pharmaceutical ingredient manufacturer for deviations from current Good Manufacturing Practices that were found during a recent FDA inspection.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Fourth Street Barbeque, Inc.

Product: Pick 5 Chicken & Waffle Sandwich; Mix & Match, Keep Frozen;…
Reason: Product has the potential to be contaminated with Listeria monocytogenes.
Published: June 14, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lamb Weston Inc

Product: Red Robin Burgers and Brews Crispy Onion Rings, frozen, Net…
Reason: Red Robin Burgers and Brews Crispy Onion Rings, 14 oz. retail packages, are recalled due to undeclared milk.
Published: June 14, 2017
Distribution: distributed in AR, AZ, CA, CO, IL, KS, K…

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Data last updated: September 30, 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.