Datascope recalls Cardiosave Rescue IABP model 0998-00-0800-83 due to potential battery issues that could shorten operating time. Affected units may need battery maintenance to ensure proper function.
If battery maintenance is not performed appropriately, the battery may provide less than the minimum run time of operating power. Revised labeling and training are being provided.
Datascope is recalling a specific model of intra-aortic balloon pump because improper battery maintenance could cause it to run out of power sooner than needed. This is serious for patients who rely on the device for cardiovascular support.
If battery maintenance isn't done correctly, the device might not have enough power to run for the required time. This could lead to the device failing during critical medical situations.
Patients using the Cardiosave Rescue IABP model 0998-00-0800-83 for cardiovascular support are most at risk. Healthcare providers who manage these devices may also be affected.
Check the serial number on the pump. The affected model is 0998-00-0800-83. This recall applies to all units with this specific serial number.
Ensure the battery is maintained according to the manufacturer's instructions to prevent short operating time.
The recall is for potential battery issues that could shorten operating time, but it does not cause immediate harm if maintained properly.
Check the serial number on the pump. The affected model is 0998-00-0800-83.
Ensure battery maintenance is done correctly to prevent short operating time. No immediate action is required beyond proper maintenance.
We’ve drafted a message you can send Datascope to request your refund or repair — edit it as you like.
Subject: Recall Z-1940-2019 — Datascope Datascope Hello, I own a Datascope that is covered by recall Z-1940-2019 from Datascope. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
