Datascope recalls Cardiosave Rescue Intra-Aortic Balloon Pumps with specific model numbers due to potential battery charging issues that could interrupt therapy.
IABP may lose the ability to charge batteries in one or both bay slots. Therapy may be interrupted if batteries fail to charge and the device is disconnected from AC power. Low battery alarms may alert the User to the issue prior to interruption of therapy.
Datascope is recalling Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP) with model numbers 0998-00-0800-75, 0998-00-0800-83, and 0998-00-0800-85. These devices may lose battery charge in one or both bay slots, risking therapy interruption if disconnected from AC power.
The IABP may lose the ability to charge batteries in one or both bay slots. If batteries fail to charge and the device is disconnected from AC power, therapy may be interrupted. Low battery alarms may alert users to the issue before interruption.
Patients using the Cardiosave Rescue IABP for cardiac support are most at risk. The affected units are specific model numbers sold with unique serial numbers.
Check for model numbers 0998-00-0800-75, 0998-00-0800-83, or 0998-00-0800-85 on the device. Each model has a unique serial number listed in the recall notice.
Look for low battery alarms or signs of interrupted therapy to determine if the device is functioning properly.
Reach out to Datascope Corp. for specific guidance on device status and potential remedies.
The Cardiosave Rescue IABP may lose battery charge in one or both bay slots, which could interrupt therapy if disconnected from AC power.
Check for model numbers 0998-00-0800-75, 0998-00-0800-83, or 0998-00-0800-85 on the device, each with a unique serial number listed in the recall notice.
Contact Datascope Corp. for specific guidance on device status and potential remedies.
We’ve drafted a message you can send Datascope to request your refund or repair — edit it as you like.
Subject: Recall Z-2150-2023 — Datascope Datascope Hello, I own a Datascope that is covered by recall Z-2150-2023 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.
