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Volcano Corp recalls Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
Recalled June 22, 2022 · FDA recall Z-1270-2022 · Volcano
Hazard
Due to a potential failed sterilization process. · FDA Class II
Units
11 devices
Sold at
U.S.: WA and WI O.U.S.: Canada
Description
Due to a potential failed sterilization process.
Product
Philips OmniWire Pressure guide wire REF 89185J PN 300000252891
Manufacturer(s)
Volcano Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →