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

Recall Z-0075-2022 — Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-34, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, 0998-00-0800-65

U.S. FDA — Device Enforcement · United States · 2021-09-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0075-2022
Date of alert
2021-09-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Datascope Corp.
Product category
device
Product type
Devices
Reported risk: The Helium Indicator on the Cardiosave display may over represent the amount of helium in unit in the presence of Electromagnetic Interference.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.