Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group Recalled by Datascope Corporation Due to During label reconciliation a duplicate serial number label...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Datascope Corporation directly.
Affected Products
LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group
Quantity: one unit
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 1 state: TX
About Datascope Corporation
Datascope Corporation has 67 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report