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

Recall Z-1773-2018 — POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005

U.S. FDA — Device Enforcement · United States · 2018-02-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1773-2018
Date of alert
2018-02-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bard Peripheral Vascular Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741110894
Reported risk: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
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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