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Stryker Neurovascular recalls Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090, M003W
Recalled September 19, 2018 · FDA recall Z-3020-2018 · Stryker Neurovascular
Hazard
Use-related coating damage on delivery catheter shafts of Wingspan delivery catheters were reported · FDA Class II
Units
11585
Sold at
China
Description
Use-related coating damage on delivery catheter shafts of Wingspan delivery catheters were reported
Product
Wingspan Stent System, Rx Only, Sterile EO, Catalog #: M003WE0250090, M003WE0300090, M003WE0350090, M003WE0400090, M003WE0450090, M003WE0250150, M003WE0300150, M003WE0350150, M003WE0400150, M003WE0450150, M003WE0250200, M003WE0300200, M003WE0350200, M003WE0400200, M003WE0450200
Manufacturer(s)
Stryker Neurovascular
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →