FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
FENTANYL 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
Data Explorer
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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 Trace9,872
Class I recallsReasonable probability of serious health consequences24,509
Class II recallsTemporary or medically reversible health consequences2,932
Class III recallsNot likely to cause adverse health consequencesQuick 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
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.
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A chart of recalls grouped by month.
Download CSVSummary (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
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,509 |
| Class I | 9,872 |
| Class III | 2,932 |
| Not Yet Classified | 2 |
| 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
FENTANYL 2000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
FENTANYL 100MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
FENTANYL 3000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
FENT 900MCG/SUF 210MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
FENT 600MCG/ SUF 800MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CLON 800MCG/FENT 2000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CLON 750MCG/MORP 30MG/SUF 37.5MCG/ML in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CLON 500MCG/HYDROM 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CLON 300MCG/MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CLON 100MCG/MORP 12MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
CJC-1295 2000 mcg/Ipamorelin 2000 mcg/mL Inj. in 2 mL vial Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 8MG/CLON 100MCG/HYDROM 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 7MG/HYDROM 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 675MCG/MORP 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 5MG/MORP 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 5MG/MORP 10MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 5MG/ HYDROM 15MG/ SUF 600MCG/ML (40ML) INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 4MG/FENT 3000MCG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
FDA Recall TerminatedTerminated: October 27, 2021Historical recordClass II
BUP 40MG/MORP 4MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
- Reason
- Lack of sterility assurance.
- Published
- January 22, 2020
- Distribution
- Nationwide
Data last updated:
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.