medical MODERATE Updated 2026-03-11

Datascope Corp. recalls CS300 IABP. Software Version CS300 IABP C.01.

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Recalled Product

CS300 IABP. Software Version CS300 IABP C.01.

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Hazard / Issue

The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All Model No; All UDI; All Serial No.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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