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MEDLINE ECVC7265ARecalls & reported problems

Medline Industries, Inc. · CVC 3L 7F 20CM VANTEX · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

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 16, 2026.

Recalls naming this device

  1. Jan 7, 2026Open, Classified

    Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.

    Z-2092-2026 · Root cause: Process control · FDA record ↗

  2. May 15, 2023Open, Classified

    Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.

    Z-2298-2023 · Root cause: Nonconforming Material/Component · FDA record ↗

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Sources and updates

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