ProTrack Microcatheter — Class II medical device recall Z-1442-2015
Terminated recall by Baylis Medical Corp *, reported 2015-04-22, distributed nationwide. Baylis Medical Company is recalling two lots of ProTrack Microcatheter due to the possibility that the cathete
| Recall number | Z-1442-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baylis Medical Corp *, Montreal, N/A, Canada |
| Recall initiated | 2015-03-30 |
| Classified | 2015-04-13 |
| Reported by FDA | 2015-04-22 |
| Terminated | 2016-11-17 |
| Distributed | Nationwide (US) |
| Quantity | 58 units |
| Lot numbers | CIFA080914, CIFA180814 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1442-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.