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

Recall Z-0652-2024 — Abiomed Kit, 14Fr Introducer, 13cm&25cm, Sterile Part of Pump Set (0048-0040, 0048-0045, 1000080)-Introducer(s) are intended for introduction of the Impella Catheter into the body. Part Number: 0052-3046

U.S. FDA — Device Enforcement · United States · 2023-11-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0652-2024
Date of alert
2023-11-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abiomed, Inc.
Product category
device
Product type
Devices
Reported risk: Hole(s) to the outer pouch of the Introducer Kits (both trayed and non-trayed) may compromise the sterile barrier of the Introducer Kits. Non-sterile product exposes patients to the possibility of the introduction of micro-organisms into the vasculature and/or access site, leading to an infectious process, bacteremia or sepsis
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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