Public Health Trace

Get Alerts

Data Explorer

Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

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

37,449

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,872

Class I recallsReasonable probability of serious health consequences

24,509

Class II recallsTemporary or medically reversible health consequences

2,932

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 2,096 recalls

Newest recallhttps://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-meat-and-poultry-products-due-misbranding-andPublished November 6, 2026

Most affected stateHawaii 200 recalls mention this state

Advertisement

State: NE ×
Clear all

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

Filters

Timeline Classification Table

Metric

Time range

Group by

View

Recalls announced by month (Year to date)

Download CSV

Source: FDA and USDA public dataLast updated November 7, 2026 ET

Summary (Year to date)

1,956 recalls have been announced year to date.
Oct 2026 was 4% higher than the previous complete period (Sep 2026: 209).
The highest complete period was Jun 2026 (300).
Nov 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

Recalls by class
Class	Recalls
Class II	24,509
Class I	9,872
Class III	2,932
Not Yet Classified	2

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Immunexx, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0270, NDC 73069-244-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Arthros, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0030, NDC 73069-035-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-GI, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0211, NDC 73069-189-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Mesenchyme, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0092, NDC 73069-102-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Lymph 1, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0370, NDC 73069-310-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Prolo, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0558, NDC 73069-443-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Collagen, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0085, NDC 73069-095-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Infla, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0279, NDC 73069-249-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Neuro 3, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0463, NDC 73069-373-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Articula, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0031, NDC 73069-037-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Systemic Detox, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0665, NDC 73069-500-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Adipose, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0008, NDC 73069-024-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Ithurts, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0290, NDC 73069-270-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Ouch, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0500, NDC 73069-402-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-MuSkel-Neural, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC4020, NDC 73069-347-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: December 10, 2020Historical recordClass II

Viatrexx-Connectissue, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0090, NDC 73069-100-41.

by 8046255 Canada Inc. DBA Viatrexx

Reason: Lack of Assurance of Sterility: products manufactured in a manner than cannot guarantee its sterility.
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: August 18, 2020Historical recordClass III

Motion Sickness Strips (meclizine hydrochloride) 25 mg strips, 8-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 69842-288-01. UPC 5042849946

by Sato Pharmaceutical Inc.

Reason: Subpotent Drug
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: August 18, 2020Historical recordClass III

WAL-DRAM 2 (meclizine Hydrochloride) 25 mg tablets, packaged in a) 12 count (NDC 0363-1407-01, UPC 3 11917-18328 2 ) and b) 18-count boxes (NDC 0363-1407-02, UPC 3 11917-20318 8) Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501,

by Sato Pharmaceutical Inc.

Reason: Subpotent Drug
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: August 18, 2020Historical recordClass III

Motion Sickness (meclizine hydrochloride) 25 mg tablets, 12-count box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 59779-534-01. UPC 050428345535

by Sato Pharmaceutical Inc.

Reason: Subpotent Drug
Published: November 20, 2019
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: August 18, 2020Historical recordClass III

Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 49873-803-01. UPC 4987301603

by Sato Pharmaceutical Inc.

Reason: Subpotent Drug
Published: November 20, 2019
Distribution: Nationwide

View recall →

Data last updated: November 7, 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.