FDA Device recall Z-1442-2015
ProTrack Microcatheter
- FDA Device
- Class II
- terminated
- Published 2015-04-22
On 2015-04-22 the FDA classified a Class II recall of ProTrack Microcatheter by Baylis Medical, citing baylis Medical Company is recalling two lots of ProTrack Microcatheter due to the possibility that the catheter may have circumferential defects along its shaft.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1442-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-30 |
| Published | 2015-04-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baylis Medical |
| Distribution | US |
Product
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.
Reason
Baylis Medical Company is recalling two lots of ProTrack Microcatheter due to the possibility that the catheter may have circumferential defects along its shaft.
Identifiers
| code_info | Lots CIFA180814 and CIFA080914 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1442-2015%22
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