Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1404-2015 — Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.

U.S. FDA — Device Enforcement · United States · 2015-03-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1404-2015
Date of alert
2015-03-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: Package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drainage system.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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