Baylis Medical Corp * Recalls

Overview of recall records associated with Baylis Medical Corp *, including dates, categories and classifications where available.

2recall records

Nov 16, 2016latest record date

Dec 9, 2015earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceNov 16, 2016

Baylis Medical Corp * NRG Transseptal Needle and NRG RF Transseptal Kit recall — FDA Z-0393-2017

The firm is voluntarily recalling lots of the NRG Transseptal Needle and NRG RF Transseptal Kit due to the possibility for an integrity defect to the Tyvek pouch of the NRG Transseptal…

Class IIFDA: TerminatedBaylis Medical Corp *

Medical DeviceDec 9, 2015

Baylis Medical Corp * ProTrack Microcatheter recall — FDA Z-0356-2016

Microcatheter may have circumferential defects (cracks) along its shaft.

Class IIFDA: TerminatedBaylis Medical Corp *

Understanding this recall history

This page summarizes recall records in which the official source identifies Baylis Medical Corp * as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.