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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: AS ×
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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

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 II

Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5 mg per 5 mL, 473 mL bottles, Rx only, Mfd. by: KVK-Tech, Inc. Newtown PA 18940; NDC 10702-150-16

by KVK-Tech, Inc.

Reason: Presence of Foreign Substance: Black particles were found in the lots during retain sample inspection
Published: November 20, 2019
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Viatrexx-ANS/CNS, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0025, NDC 73069-039-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Male+, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0400, NDC 73069-320-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Neuro, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0460, NDC 73069-375-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Hair, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0251, NDC 73069-206-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Facial, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0184, NDC 73069-164-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Intra-Cell, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0280, NDC 73069-250-41.

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

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FDA Recall Terminated Historical recordClass II

Viatrexx-Relief +, 10 mL Sterile multi-dose vial, Rx only, Viatrexx Bio Incorporated, Newark, DE, USA, 19713, Item: VSPC0615, NDC 73069-450-41.

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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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

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FDA Recall Terminated Historical 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 →

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.