FDA Device recall Z-2568-2014
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
- FDA Device
- Class III
- terminated
- Published 2014-09-10
On 2014-09-10 the FDA classified a Class III recall of LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group by Datascope, citing during label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2568-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2014-08-11 |
| Published | 2014-09-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Datascope |
| Distribution | TX |
Product
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
Reason
During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.
Identifiers
| code_info | Part Number - 0684-00-0480-01U |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2568-2014%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.