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Medical Device

CS300 IABP. Software Version CS300 IABP C.01.

Recall date: 2026-03-11 · Source: FDA_DEVICE
Brand / Firm
Datascope Corp.
Product
CS300 IABP. Software Version CS300 IABP C.01.
Reason for recall
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
Units affected
10,897 units
Description
CS300 IABP. Software Version CS300 IABP C.01.
View official recall notice →