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

Recall Z-2235-2016 — T100-022WF, IV Set with 2 Y-Sites, 0.22 micron filter, Back Check Valve, & FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

U.S. FDA — Device Enforcement · United States · 2016-06-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2235-2016
Date of alert: 2016-06-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: WalkMed Infusion, LLC
Product category: device
Product type: Devices

Reported risk: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton Administration Sets Due to the Potential Presence of Particulate In or On the Administration Sets.

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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Recall Z-2235-2016 — T100-022WF, IV Set with 2 Y-Sites, 0.22 micron filter, Back Check Valve, & FP Clip. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.

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