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

Recall Z-1108-2015 — AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the water

U.S. FDA — Device Enforcement · United States · 2015-01-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1108-2015
Date of alert: 2015-01-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Teleflex Medical
Product category: device
Product type: Devices

Reported risk: The packages may contain foreign material (black particles).

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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