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Recall totals

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

37,115

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,793

Class I recallsReasonable probability of serious health consequences

24,343

Class II recallsTemporary or medically reversible health consequences

2,887

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/so-delicious-dairy-freer-issues-voluntary-recall-salted-caramel-cluster-non-dairy-frozen-dessertPublished September 15, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 16, 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	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,343
Class I	9,793
Class III	2,887
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

Sirolimus Oral Solution, 1 mg/mL, 60 mL bottle, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326, NDC 60505-6197-2

by Apotex Corp.

Reason: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to lot RZ1598 exceeded the specification limit at the 14-month timepoint.
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nitrofurantoin Capsules, USP (Monohydrate/Macrocrystals), 100 mg, 100 Capsules (10 x 10), 10-count blisters per card, 10 cards per carton, Unit Dose NDC 68084-446-11, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 68084-446-01

by American Health Packaging

Reason: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to dissolution failure at 0-time of the repackaged lot. Drug release results were above specification at 0-time.
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

GaviLyte -C (Polyethylene Glycol 3350, 240 g) and electrolytes for Oral Solution, USP with flavor pack NDC# 43386-060-19

by Lupin Pharmaceuticals Inc.

Reason: Failed Stability Specification
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 40 mg, 90 Tablets, Rx only NDC 0071-0535-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 20 mg, 90 Tablets, Rx only NDC 0071-0532-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Accupril (Quinapril HCl Tablets) 10 mg, 90 Tablets Rx only NDC 0071-0530-23 Distributed by: Parke-Davis Division of Pfizer Inc. NY, NY 10017

by Pfizer Inc.

Reason: CGMP Deviations: Contains N-nitrosoquinapril above the acceptable limits.
Published: May 25, 2022
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Atlanta Cheesecake Company LLC

Product: SE Grocers Cheesecake SAMPLER New York Style, Chocolate Silk…
Reason: The firm was notified by a customer that the label does not declare pecans in its ingredient statement.
Published: May 25, 2022
Distribution: Product was shipped to distributors the…

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FDA Recall United States Terminated Historical recordClass I

T Fresh Company DBA Yes Produce

Product: Yes! Enoki Mushrooms; Pesticide Free Produce: Vacuumed pack…
Reason: California Department of Public Health sampled product with a result of Listeria monocytogenes
Published: May 25, 2022
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

Driscoll's Inc.

Product: Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz…
Reason: California Department of Pesticide Regulation detected the presence of Formetante HCI. This pesticide has a non-tolerance for blackberries.
Published: May 25, 2022
Distribution: Product shipped to 13 DC's located in CA…

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FDA Recall Terminated Historical recordClass III

Nandrolone Decanoate, USP, 1 kg per plastic container, Rx Only, For Prescription Compounding, Distributed by: Humco, 7400 Alumax Road, Texarkana, TX 75501. NDC 0395-8212-43

by Fagron, Inc

Reason: Subpotent Drug
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nandrolone Decanoate, USP, 500 g per plastic container, Rx Only, For Prescription Compounding, Distributed by: Humco, 7400 Alumax Road, Texarkana, TX 75501. NDC 0395-8212-56

by Fagron, Inc

Reason: Subpotent Drug
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nandrolone Decanoate, USP, 1 kg per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-07

by Fagron, Inc

Reason: Subpotent Drug
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nandrolone Decanoate, USP, 500 g per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-05

by Fagron, Inc

Reason: Subpotent Drug
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Nandrolone Decanoate, USP, 100 g per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-04

by Fagron, Inc

Reason: Subpotent Drug
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Esomeprazole Magnesium Delayed-Release Capsules, USP 40 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-010-16

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Esomeprazole Magnesium Delayed-Release Capsules, USP 20 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-009-16

by Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Reason: Failed Impurities/Degradation Specifications: OOS result was obtained for Any Other Individual Impurity at the 12M room temperature time point.
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg, 60-count bottle, Rx only Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 47335-738-86

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 150 mg packaged in a) 60-count bottle (47335-737-86), b)100-count bottle (47335-737-88), c)500-count bottle (47335-737-13), Rx only Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512, Manufactured by: Sun Pharmaceutical Industries Limited, Halol-Baroda Highway, Halol-389 350, Gujarat, India

by SUN PHARMACEUTICAL INDUSTRIES INC

Reason: Presence Of Foreign Substance: Customer complaint for the presence of dark, gritty substance found within the bottle which was determined to be activated carbon from the desiccant canister inside the bottle.
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Completed Historical recordClass I

SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.

by Fagron, Inc

Reason: Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.
Published: May 18, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, NDC 55513-0206-01

by Amgen, Inc.

Reason: Defective container: loose crimp defect, potential loss of container integrity.
Published: May 18, 2022
Distribution: Nationwide

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Data last updated: September 16, 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.