Datascope recalls CS300 Intra-Aortic Balloon Pump (serial numbers 0998-00-3023-55) due to potential battery failure if not maintained properly. Affected users should contact for remedy.
If battery maintenance is not performed per instructions, the battery may provide less than the minimum run time of operating power.
Datascope is recalling its CS300 Intra-Aortic Balloon Pump (serial number 0998-00-3023-55) because improper battery maintenance could cause the pump to run out of power. This is serious for patients relying on the device for cardiovascular support.
If battery maintenance isn't done as instructed, the battery might not last long enough for the pump to function properly. This could lead to the pump stopping during critical medical use.
Patients using the CS300 Intra-Aortic Balloon Pump for cardiovascular support are most at risk. The recall affects specific serial numbers sold in the U.S.
Check for the serial number 0998-00-3023-55 on the pump. The device is for cardiovascular use and operates on 220V power.
Review the device's manual for proper battery care to ensure it functions correctly.
No, only specific serial number 0998-00-3023-55 is affected.
Contact Datascope for remedy instructions as the recall remedy is not specified in the record.
Only if you follow battery maintenance instructions; otherwise, the pump may stop working unexpectedly.
We’ve drafted a message you can send Datascope to request your refund or repair — edit it as you like.
Subject: Recall Z-1944-2019 — Datascope Datascope Hello, I own a Datascope that is covered by recall Z-1944-2019 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.
