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Recall totals

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

37,324

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,859

Class I recallsReasonable probability of serious health consequences

24,440

Class II recallsTemporary or medically reversible health consequences

2,900

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 2,095 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/kayem-foods-inc--recalls-meat-and-poultry-products-due-possible-temperature-abusePublished October 17, 2026

Most affected stateHawaii 200 recalls mention this state

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

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Source: FDA and USDA public dataLast updated October 21, 2026 ET

Summary (Year to date)

1,739 recalls have been announced year to date.
Sep 2026 was 15% higher than the previous complete period (Aug 2026: 182).
The highest complete period was Jun 2026 (300).
Oct 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

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Recalls by class
Class	Recalls
Class II	24,440
Class I	9,859
Class III	2,900
Not Yet Classified	2

FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Glimepiride, USP, 4 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0250-30; b) 90-count bottle, NDC 61919-0250-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Glimepiride, USP, 2 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0488-30; b) 90-count bottle, NDC 61919-0448-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Glimepiride, USP, 1 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0723-30; b) 90-count bottle, NDC 61919-0723-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Ropinirole, USP, 1 mg Tablets, Rx Only, Packaged as a 30-count bottle, NDC 72189-0364-30; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Ropinirole, USP, 0.25 mg Tablets, Rx Only, Packaged as a 30-count bottle, NDC 72189-0364-30; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Finasteride, USP, 5 mg Tablets, Rx Only, Packaged as a 90-count bottle, NDC 61919-0733-90; Packaged and Distributed By: Direct Rx

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: June 17, 2024Historical recordClass II

Montelukast Sodium Tablets, USP, 10 mg Tablets, Rx Only, Packaged as: a) 30-count bottle, NDC 61919-0009-30; b) 90-count bottle, NDC 61919-0009-90; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534

by Direct Rx

Reason: cGMP deviations
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall TerminatedTerminated: November 8, 2024Historical recordClass II

Calcitonin Salmon Nasal Spray, USP, 2200 International Units per mL corresponding to 200 International Units/spray, 3.7 mL bottle, Rx only, Manufactured by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 49884-161-11.

by Endo Pharmaceuticals, Inc.

Reason: Failed Impurities/Degradation Specifications and Subpotent Drug: High Out of Specification results for a known and unknown impurity as well as low Out of Specification results for assay.
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: May 2, 2023Historical recordClass I

THE ISH COMPANY

Product: ISH Shrimpish Sample Meal Kit: ( Sample Meal Kit ) a package…
Reason: undeclared soy proteins
Published: April 5, 2023
Distribution: Multiple states

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FDA Recall United States TerminatedTerminated: January 15, 2025Historical recordClass II

BINDLE BOTTLE

Product: Stainless Steel Water Bottle The product comes in four sizes…
Reason: Water bottle has a cup with a screw cap attached by a weld that has been found to leach lead.
Published: April 5, 2023
Distribution: Nationwide

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Seaweed distributed in un-labeled plastic container…
Reason: Seasoned Seaweed was recalled due to undeclared Sesame Seeds, Wheat, Y5, and B1.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Hot Pepper in Soy Sauce distributed in un-labeled plastic co…
Reason: Hot Pepper in Soy Sauce was recalled due to undeclared Soybean and Wheat.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Green Laver distributed in un-labeled plastic conta…
Reason: Seasoned Green Laver was recalled due to undeclared Soybean, Wheat, Fish (Anchovy), and Sesame Seeds.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Stir-Fried Dried Squid distributed in un-labeled plastic con…
Reason: Stir-Fried Dried Squid was recalled due to undeclared Milk, Wheat, and Soybean.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass III

Lemonland Food Corp

Product: Cucumber Pickle distributed in un-labeled plastic containers…
Reason: Cucumber Pickle was removed because the firm provided the updated ingredients statement to consignees. Product does not contain any allergens.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Lotus Root distributed in un-labeled plastic contai…
Reason: Seasoned Lotus Root was recalled due to undeclared Soybean and Wheat.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Fish Meat distributed in un-labeled plastic contain…
Reason: Seasoned Fish Meat was recalled due to undeclared Fish (Pollock, Golden Threadfin Bream, Hairtail, Lizard Fish), Wheat, and Soy bean.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Crab was distributed in un-labeled plastic containe…
Reason: Seasoned Crab recalled due to undeclared Crab, Sesame Seeds, and fish (Anchovy).
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Dried Pollack distributed in un-labeled plastic con…
Reason: Seasoned Dried Pollack was recalled due to undeclared Fish (Pollack), Wheat, Soybean.
Published: April 5, 2023
Distribution: Distributed in Washington

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FDA Recall United States TerminatedTerminated: March 29, 2023Historical recordClass II

Lemonland Food Corp

Product: Seasoned Radish Sliced distributed in un-labeled plastic con…
Reason: Seasoned Radish Sliced was recalled due to undeclared Fish (Anchovy, Big Eye Herring), Crustacean (Shrimp), Sesame.
Published: April 5, 2023
Distribution: Distributed in Washington

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Data last updated: October 21, 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.