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

Recall Z-1147-2023 — Cardiosave Hybrid 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 0998-UC-0800-31* 0998-UC-0800-33* 0998-UC-0800-52* 0998-UC-0800-53* 0998-00-0800-55* * --

U.S. FDA — Device Enforcement · United States · 2023-02-07 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1147-2023
Date of alert
2023-02-07
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Datascope Corp.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10607567109053
Reported risk: An unexpected shutdown of the IABP may occur due to loss of communication between the Executive Processor PCBA and the Video Generator PCBA. This may result in an interruption to therapy which may threaten the hemodynamic stability of the supported patient as the user is left unaware to the status of the Cardiosave IABP.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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