Skip to content

PLEUR-EVAC IPN028459Recalls & reported problems

Teleflex Incorporated · THORACIC CATHETER RIGHT ANGLE 32 FRENCH SOFT · Class 1

All models of PLEUR-EVAC (15)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Feb 12, 2021Class IITerminated

    Teleflex is recalling this product due to a lack of assurance of sterility.

    Z-1298-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other CATHETER, IRRIGATION devices

All CATHETER, IRRIGATION devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page