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

Recall Z-0898-2013 — REF CMS-CT6T225, 6F Triple Lumen CT PICC with M.S.T. Components Product Usage: Power injectable infusion PICC insertion kits

U.S. FDA — Device Enforcement · United States · 2012-12-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0898-2013
Date of alert
2012-12-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medical Components, Inc dba MedComp
Product category
device
Product type
Devices
Reported risk: The affected product was packaged with the incorrect introducer needle. The kit label indicates a "safety" needle is included; the kits were packaged with a non-safety needle.
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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