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Baylis Medical Corp * recalls ProTrack Microcatheter. Model/Catalog Numbers CIC38-145, CIC35-145. Sterile, single use device intended to be used as
Recalled December 9, 2015 · FDA recall Z-0356-2016 · Baylis Medical Corp *
Hazard
Microcatheter may have circumferential defects (cracks) along its shaft. · FDA Class II
Units
433 units
Sold at
Nationwide Distribution.
Description
Microcatheter may have circumferential defects (cracks) along its shaft.
Product
ProTrack Microcatheter. Model/Catalog Numbers CIC38-145, CIC35-145. Sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires. Coaxial Injectable catheter guide wire. Cardiovascular.
Manufacturer(s)
Baylis Medical Corp *
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →