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

Recall Z-2003-2014 — Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .

U.S. FDA — Device Enforcement · United States · 2014-06-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2003-2014
Date of alert
2014-06-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Teleflex Medical
Product category
device
Product type
Devices
Reported risk: The seals of the respiratory gas humidifier adaptor packaging may be creased which may potentially affect packaging integrity.
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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