FDA Device recall Z-1507-2021
Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons
- FDA Device
- Class III
- ongoing
- Published 2021-05-05
On 2021-05-05 the FDA classified a Class III recall of Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons by Datascope, citing there are cybersecurity vulnerabilities in a widely used low-level TCP/IP software library that may result in a loss of communication to the Hospital Information System/Clinical I….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1507-2021 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2021-03-22 |
| Published | 2021-05-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Datascope |
| Distribution | US |
Product
Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provides temporary support to the left ventricle via the principle of counterpulsation, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Reason
There are cybersecurity vulnerabilities in a widely used low-level TCP/IP software library that may result in a loss of communication to the Hospital Information System/Clinical Information System (HIS/CIS).
Identifiers
| code_info | All Systems. UDI: 10607567112312 10607567108407 10607567113449 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1507-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.