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Recall totals

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

37,066

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,786

Class I recallsReasonable probability of serious health consequences

24,313

Class II recallsTemporary or medically reversible health consequences

2,876

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/whole-foods-market-issues-allergy-alert-undeclared-egg-cabricharme-cheesePublished September 11, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 13, 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	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,313
Class I	9,786
Class III	2,876
Not Yet Classified	2

FDA Recall United States Terminated Historical recordClass II

Sanders Candy LLC dba Second Nature Brands

Product: Sanders Milk Chocolate Sea Salt Pecan Cluster: 0-35900-25550…
Reason: Foreign material in product. Pieces of cleaning brush bristles found in the product
Published: January 18, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sanders Candy LLC dba Second Nature Brands

Product: Sanders Milk Chocolate Sea Salt Caramels: UPC 0-35900-27636-…
Reason: Foreign material in product. Pieces of cleaning brush bristles found in the product
Published: January 18, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sanders Candy LLC dba Second Nature Brands

Product: Sanders Assorted Milk and Dark Sea Salt Caramels UPC 0-35900…
Reason: Foreign material in product. Pieces of cleaning brush bristles found in the product
Published: January 18, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Sanders Candy LLC dba Second Nature Brands

Product: Sanders Dark Chocolate Sea Salt Caramels: UPC 0-35900-26442-…
Reason: Foreign material in product. Pieces of cleaning brush bristles found in the product
Published: January 18, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Epi-Caine, Epinephrine 0.025% Lidocaine HCL 0.75% Solution for Intraocular Injection, 1 ml, Single Dose Vial, Compounded by Pine Pharmaceuticals, 355 Riverwalk Pkwy, Tonawanda, NY 14150. NDC 69194-0948-1

by Pine Pharmaceuticals, LLC

Reason: CGMP Deviations: Raw material recalled by repackager, due to discoloration.
Published: January 11, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride Injection, 1,000 mL bags, a) Case (NDC 0409-7620-59), b) Single Unit (NDC 0409-7620-49), Rx only, Distributed By Hospira, Inc., Lake Forest, IL 60045 USA,

by Pfizer Inc.

Reason: Lack of assurance of sterility: Bags have the potential to leak.
Published: January 11, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Prochlorperazine Maleate Tablets, USP 5mg, 100 tablets, RX Only, Jubilant Cadista Pharmaceuticals, Inc., Salisbury, Maryland 21801, NDC 59746-113-06

by Jubilant Cadista Pharmaceuticals, Inc.

Reason: Subpotent Drug: Out of specification for assay at the 18-month stability timepoint.
Published: January 11, 2023
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL); Single Dose 20mL Vial, Rx only, Distributed by: AuroMedics Pharma LLC, 279 Princeton-Hightstown Rd, E. Windsor, NJ 08520; Made in India. NDC 55150-155-20

by Eugia US LLC

Reason: Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Published: January 11, 2023
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Cranberry Sweets & More Inc

Product: Recalled Meltaways product is packaged in clear cellophane b…
Reason: Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Published: January 11, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL, Rx Only, Mfg by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Mfg for: Apotex Corp. Weston, FL 33326, NDC 60505-1005-4

by Apotex Corp.

Reason: Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.
Published: January 4, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile Solution, packaged as a a) 2.5 gallon bottle (9,464 ml), NDC 55533-524-02, and b) 55 gallon bottle (208,198 ml), NDC 55533-524-03, Manufactured for: Multi-Mist Products A Division of NCH Corporation 1618 Northgate, Irving, Texas 75062

by NCH Life Sciences LLC

Reason: CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
Published: January 4, 2023
Distribution: Nationwide

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FDA Recall Completed Historical recordClass II

Glycopyrrolate Tablets, USP, 1 mg, 50 Tablets (5x10) Unit Dose carton, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-363-15

by AVKARE LLC

Reason: Failed impurities/degradation specifications: Out of specification for unknown impurities.
Published: January 4, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Ganciclovir for Injection, USP, 500mg per vial, packaged in a 10-count carton, Rx Only, Mfd. by: THYMOORGAN PHARMAZIE GmbH, Germany, Distributed by Hikma Berkeley Heights, NJ 07922, NDC 0143-9299-01

by Hikma Pharmaceuticals USA Inc.

Reason: Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Published: January 4, 2023
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Quinapril Tablets USP, 20 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-558-09

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published: December 28, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Quinapril Tablets USP, 40 mg (90 pack), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202, by: Lupin Limited, Goa 403 722 India, NDC# 68180-554-09

by Lupin Pharmaceuticals Inc.

Reason: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Published: December 28, 2022
Distribution: Nationwide

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FDA Recall Ongoing Historical recordClass II

Glycopyrrolate Tablets, USP, 1 mg, 100 tablets, Rx Only, Distributed by: Aurobindo Pharma USA, Inc., East Windsor, NJ 08520, NDC 13107-014-01

by Aurolife Pharma, LLC

Reason: Failed Impurities/Degradation Specifications
Published: December 28, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Oxcarbazepine Tablets 600mg, packaged in a) 100- count bottles (NDC 62756-185-88), b) 500-count bottles (NDC 62756-185-13), c)1000-count bottles (NDC 62756-185-18), 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
Published: December 28, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured By: HETERO LABS LIMITED, Jeedimetla, Hyderabad - 500 055, India, NDC 31722-627-26

by Camber Pharmaceuticals, Inc

Reason: Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content
Published: December 21, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Menastil, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Mfg. for/Dist. By Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-711-01.

by Atlantic Management Resources Ltd.

Reason: cGMP Deviations
Published: December 21, 2022
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

ProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by: Endometriosis Assoc. Inc. (International), Mfg. by Claire Ellen Topicals, P.O. Box 901 Westborough, MA 01581, USA, NDC# 66233-712-01.

by Atlantic Management Resources Ltd.

Reason: cGMP Deviations
Published: December 21, 2022
Distribution: Nationwide

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Data last updated: September 13, 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.