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

POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1678300 — recall Z-1764-2018

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-1764-2018
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)
00801741110801
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.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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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