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Datascope Corporation recalls BO-TOP 20705 SMALL PATIENT 1/4, Catalog No. 701053486
Recalled May 16, 2018 · FDA recall Z-1713-2018 · Datascope
Hazard
The Better Bladder device provided as part of some custom tubing kits has been recalled by its manufacturer. Seal separation from the housing may allow air to enter the housing and collapse the balloon. This may increase resistance to flow in the venous line and cause a drop in ECMO circuit blood flow. · FDA Class II
Units
10
Sold at
Distributed to accounts in AL, AR, CA, DC, FL, IL, LA, MO, NC, PA, SC, TX, and WA.
Description
The Better Bladder device provided as part of some custom tubing kits has been recalled by its manufacturer. Seal separation from the housing may allow air to enter the housing and collapse the balloon. This may increase resistance to flow in the venous line and cause a drop in ECMO circuit blood flow.
Product
BO-TOP 20705 SMALL PATIENT 1/4, Catalog No. 701053486
Manufacturer(s)
Datascope Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →