MCI MCITX-1Recalls & reported problems
Vygon Corporation · MAXIMUM BARRIER TRAY · Class 2
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Feb 28, 2018Terminated
Potential friction holes may affect the sterility of the product.
Z-1638-2018 · Root cause: Under Investigation by firm · FDA record ↗
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- LSL HEALTHCARE 2519CPLSL Industries, LLC · Peripheral catheter insertion kit1 recall0 reports
- CARDINAL HEALTH PVMHIVM15Cardinal Health 200, LLC · Peripheral catheter insertion kit1 recall0 reports
- VYGON AMS-8010CP-1Vygon Corporation · Peripheral catheter insertion kit1 recall0 reports
- VYGON AMS-9093CPVygon Corporation · Peripheral catheter insertion kit1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.