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

Recall Z-1803-2012 — Churchill Medical Systems, Inc. PORT-A-CATH Tray Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens

U.S. FDA — Device Enforcement · United States · 2012-05-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1803-2012
Date of alert
2012-05-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Vygon Corporation
Product category
device
Product type
Devices
Reported risk: Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes.
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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