FDAMarch 3, 2017device
ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide wire is a smooth, stainless steel wire, with a silicone coating, and a radiopaque distal spring tip. The guide wire allows for proper positioning of the device crown within peri...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Cardiovascular Systems, Inc. is recalling one lot of ViperWire Advance with Flextip, model VPR-GW-FT18 because it may contain a 0.014" ViperWire Advance Flextip product instead of the 0.018" ViperWire Advance with Flextip.
What to do
FDA enforcement status: Terminated
Brands named
cardiovascular systemscardiovascular
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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