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Recall totals

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

37,135

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 recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated September 23, 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 United States Terminated Historical recordClass II

Plant Devas Inc

Product: Clay Mask Kit; 2 glass jars of clay: Green Tea Clay 0.3 oz.…
Reason: FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Kodiak Cakes, LLC

Product: Kodiak Cakes, Energy Waffles, Blueberry Chia, Net Wt 10.72 O…
Reason: The frozen waffle product contains whey but fails to declare the major food allergen "milk" on the label
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product: Xenesta Nuvive Womens 90 count packaged in a white plastic b…
Reason: Recalled dietary supplements may contain undeclared milk.
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product: Xenesta Nuvive Mens 90 count packaged in an white plastic bo…
Reason: Recalled dietary supplements may contain undeclared milk.
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product: Thyroid Resilience 120 count bottle packaged in an amber pla…
Reason: Recalled dietary supplements may contain undeclared milk.
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Progressive Laboratories, Inc

Product: Testosterzone 180 count bottle packaged in an amber plastic…
Reason: Recalled dietary supplements may contain undeclared milk.
Published: March 21, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

RANITIDINE Tablets, USP 150 mg UD 100 tablets (10x10), RX Only, Manufactured by: Amneal Pharmaceuticals, Hauppauge, NY 11788, NDC 63739-489-10

by Mckesson Packaging Services

Reason: Failed Stability Specifications
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Lynparza (olaparib) capsules 50 mg, 112 count bottles, Rx only, Manufactured for: Astra Zeneca Pharmaceuticals LP Wilmington, DE 19850 by: Patheon Pharmaceuticals, Inc. Cincinnati OH 45237 Product of Switzerland NDC 0310-0657-58

by AstraZeneca Pharmaceuticals LP

Reason: Failed Impurities/Degradation Specifications; elevated levels of quality attribute Form L (polymorph).
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Methylphenidate Hydrochloride Extended-release Tablets, USP, 36 mg, 100-count bottle, Rx only, Trigen Laboratories, LLC Bridgewater, NJ 08807. NDC 13811-708-10

by Osmotica Pharmaceutical Corp

Reason: Subpotent Drug:100-count product bottle labeled as Methylphenidate HCL ER Tablets 36 mg found to contain 1 27 mg Methylphenidate HCL ER Tablet.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atropine Sulfate Ophthalmic 1% Solution, USP, 5mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-215-05

by Akorn, Inc.

Reason: Failed Stability Specification: OOS low viscosity results discovered during retain testing.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Labetalol Hydrochloride Injection, USP, 100 mg/ 20 mL (5 mg/mL), 20 mL Multidose Vial, Rx only, labeled as a) Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-20; and b) NOVAPLUS, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2267-25.

by Hospira Inc. A Pfizer Company

Reason: Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass I

Lotte International America Corp.

Product: Lotte Kancho Choco-Biscuit; Sold as Lotte Kancho - 42 g…
Reason: Firm was notified by customer of peanut allergen found in the product during product sampling and testing in Kancho Choco Biscuits.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall United States Ongoing Historical recordClass II

Snyder's-Lance Inc.

Product: Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable po…
Reason: Snyder's Lance is voluntarily recalling 6.5 oz. Emerald brand walnuts due to the presence of undeclared peanuts, almonds, cashews, and pecans.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Vitalab Co Inc

Product: Product packaged in the following ways A) Sonne's, No. 17, N…
Reason: The firm's vitamin C dietary supplement contains lactose, a milk-derived ingredient, but fails to declare the major food allergen "milk" on the label.
Published: March 14, 2018
Distribution: Product distributed to consumers, distri…

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FDA Recall United States Terminated Historical recordClass II

Get The Tea

Product: Life Change Fat Burner, 90 Gel Caps!, Burn Fat!, Remove fat…
Reason: Get The Tea is notifying customers that Life Change Fat Burners contain soy.
Published: March 14, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 50 mL Single-Use flexible container, Rx Only, Manufactured for: AuroMedics Pharma LLC 6 Wheeling Drive, Dayton, NJ 08810 Manufactured for: Aurobindo Pharma Limited IDA, Pashamylaram - 502307, India ---- NDC 55150-243-46

by AuroMedics Pharma LLC

Reason: Presence of Particulate Matter; contains visible particulate matter identified as mold.
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass I

GERICARE Eyewash, sterile eye irrigating solution, packaged in a 4 fl oz (118 mL) bottle, OTC, Distributed by Geri-Care Pharmaceuticals Corp., Brooklyn, NY 11204, NDC 57896-0186-04

by Kareway Products Inc

Reason: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Irrigation USP, 1000 mL Plastic Irrigation Container (PIC), Rx only, B. Braun Medical Inc., Irvine, CA 92614, Catalog # R5200-01, NDC 0264-2201-00.

by B. Braun Medical Inc

Reason: Presence of Particulate Matter: Customer complaint of particulate matter which has been identified as polyethylene, which is consistent with the material used to manufacture the container cap was received.
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

SyrSpend SF Suspending Base, a) 500 mL (NDC 51552-1079-5) and b) 4 L (NDC 51552-1079-9), Rx Only, Manufactured by Fagron Inc. St. Paul, MN 55120

by Fagron, Inc

Reason: Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).
Published: March 7, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

PVP Scrub Solution, Povidone Iodine, 7.5% (equivalent to 0.75% available iodine), 4 FL OZ bottle, Manufactured in USA by Medline Industries, Inc., Northfield, IL 60093; Product Number MDS093945; NDC 53329-938-04

by Medline Industries Inc

Reason: Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
Published: March 7, 2018
Distribution: Nationwide

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Data last updated: September 23, 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.