Baylis Medical Corp *: Medical Device Recall in 2015 - (Recall #: Z-1442-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires.

Product Classification:

Class II

Date Initiated: March 30, 2015

Date Posted: April 22, 2015

Recall Number: Z-1442-2015

Event ID: 70896

Reason for Recall:

Baylis Medical Company is recalling two lots of ProTrack Microcatheter due to the possibility that the catheter may have circumferential defects along its shaft.

Status: Terminated

Product Quantity: 58 units

Code Information:

Lots CIFA180814 and CIFA080914

Distribution Pattern:

US Nationwide Distribution - US Nationwide in the states of MO, MA, OH, CA, AR, MA, FL, GA, CO, TX, KY, NY, MI, WI, OR

Voluntary or Mandated:

Voluntary: Firm initiated