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Datascope Corporation recalls LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
Recalled September 10, 2014 · FDA recall Z-2568-2014 · Datascope
Hazard
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. · FDA Class III
Units
one unit
Sold at
US Distribution to TX.
Description
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.
Product
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
Manufacturer(s)
Datascope Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →