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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

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Recalls announced by month (Year to date)

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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: October 27, 2021Historical recordClass II

MORPHINE 6MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 4MG/ML INJ in 20mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 30MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 2MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 18MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 15MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORPHINE 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

MORP 20MG/SUF 70MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 6MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 4MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 3MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROMORPHONE 15MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HYDROM 10MG/SUF 200MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HCG 10,000U/1ML INJ in 4 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

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FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

HCG 1,000U/1ML INJ in 4 mL vial Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
Distribution: Nationwide

View recall →

FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II

FENTANYL 800MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

by Assurance Infusion

Reason: Lack of sterility assurance.
Published: January 22, 2020
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.