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Recall totals

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

37,206

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/frutas-y-hortalizas-del-sur-sa-expands-recalls-include-additional-lots-great-value-frozen-organicPublished October 2, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 2, 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).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

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 United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: R&H Speedy Creme Vanilla Filling Mix Item 01148908 25 pou…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mi…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Dawn Food Products Inc.

Product: QUIK 'N CREAMY VANILLA POWDERED FILLING Item number 000141…
Reason: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.
Published: April 26, 2017
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Nutiva

Product: Nutiva Nuture Vitality Organic Plant Protein Superfood 30 S…
Reason: Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Published: April 26, 2017
Distribution: Alabama, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass I

Nutiva

Product: Nutiva Nuture Vitality Organic Plant Protein Superfood 30 S…
Reason: Testing of retain sample related to a customer complaint found peanut allergen at 4.7 ppm; confirmation testing found peanut allergen at 4.8 ppm.
Published: April 26, 2017
Distribution: Alabama, California, Colorado, Connectic…

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FDA Recall United States Terminated Historical recordClass I

Pondini, inc.

Product: Pecorino Balze Volteranne DOP Societa Agricola Fattoria Li…
Reason: Pecorino Balze Volteranne raw sheeps milk cheese tested positive for Listeria monocytogenes
Published: April 26, 2017
Distribution: NJ and NY

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, packaged in a) 60-count bottles (NDC 59746-317-60) and b) 100-count bottles (NDC 59746-317-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 150 mg, packaged in a) 60-count bottles (NDC 59746-316-60) and b) 100-count bottles (NDC 59746-316-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 100 mg, packaged in a) 60-count bottles (NDC 59746-315-60) and b) 100-count bottles (NDC 59746-315-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA.

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications: high out of specification results for one of the known degradation products, m-chlorobenzoic acid.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

hydrALAZINE HYDROCHLORIDE INJECTION, USP, 20 mg/mL, 1 mL Single Dose Vial, packaged in 25 Vials per carton, Rx only, APP Fresenius Kabi USA, LLC, Lake Surich, IL 60047, NDC 63323-614-01, Distributed by McKesson Medical-Surgical, Inc.

by Mckesson Medical Surgical

Reason: Temperature Abuse: Certain pieces of these lots distributed by McKesson Medical Surgical Inc. were inadvertently stored refrigerated rather than the labeled room temperature recommendation.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lumigan (bimatoprost ophthalmic solution) 0.01%, 7.5 mL bottle, Rx only, Allergan Irvine, CA 92612, NDC 0023-3205-08.

by Allergan Sales, LLC

Reason: Failed Impurities/Degradation Specifications
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ESTRADIOL, USP Bulk (Hemihydrate), in a) 25 g (NDC 38779-2261-04) and b) 100 g (NDC 38779-2261-05) bottles, Packed by MEDISCA INC. PLATTSBURGH, NY Product Code 2261

by Medisca, Inc.

Reason: cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ESTRADIOL, USP (Hemihydrate)(Micronized), in a) 100 mg (NDC 38779-0869-07), b) 1 g (NDC 38779-0869-06), c) 5 g (NDC 38779-0869-03), d) 10 g (NDC 38779-0869-01), e) 25 g (NDC 38779-0869-04), f) 100 g (NDC 38779-0869-05) , g) 500 g (NDC 38779-0869-08), h) 1 Kg (NDC 38779-0869-09) bottles, Packed by MEDISCA INC. PLATTSBURGH, NY 12901; Product Code 0869

by Medisca, Inc.

Reason: cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ESTRONE, USP Bulk, in a) 100 mgs (NDC 38779-0891-05), b) 1 gram (NDC 38779-0891-06), c) 5 grams (NDC 38779-0891-03), d) 25 grams (NDC 38779-0891-04), and e) 100 grams (NDC 38779-0891-09) Bottles, Packed by MEDISCA INC. PLATTSBURGH, NY 12901; Product Code 0891

by Medisca, Inc.

Reason: cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ESTRIOL, USP (Micronized) Bulk, in a) 5 grams (NDC 38779-0732-03), b) 25 grams (NDC 38779-0732-04) , c) 100 grams (NDC 38779-0732-05), and d) 1 Kg (NDC 38779-0732-09) bottles, Packed by MEDISCA, INC. PLATTSBURGH, NY 12901; Product Code 0732

by Medisca, Inc.

Reason: cGMP Deviations; manufacturer initiated recall of API product after deficiencies noted during a recent FDA inspection
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Double Hyaluronic 1000, 'AN OUNCE OF GOLD' Volumizing Day Cream, Broad Spectrum SPF 30+, (Octinoxate 7.725%, Oxybenzone 6.18%, Octisalate 5.15%, Avobenzone 3.09%), Net Wt. 1.8 oz. (51 g) jar, Distributed by Signature Club A, Ltd, Tampa, FL 33609.

by Signature Club A Ltd

Reason: Microbial Contamination of Non-Sterile Products: odor complaint of product due to microbial contamination.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12

by Akorn, Inc.

Reason: Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Published: April 19, 2017
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Levonorgestrel Non-Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-012-01),

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason: cGMP Deviations; lack of quality assurance.
Published: April 19, 2017
Distribution: Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Ethinyl Estradiol Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China (NDC 44132-002-05)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason: cGMP Deviations; lack of quality assurance.
Published: April 19, 2017
Distribution: Product distributed to NY, TX, SC, CO, M…

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FDA Recall Terminated Historical recordClass II

Testosterone Micronized, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd., Qinhuangdao 066004, China (NDC 44132-006-06)

by Qinhuangdao Zizhu Pharmaceutical, Co.

Reason: cGMP Deviations; lack of quality assurance.
Published: April 19, 2017
Distribution: Product distributed to NY, TX, SC, CO, M…

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Data last updated: October 2, 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.