FDA recall Z-2795-2020

Bioseal Corporation · Class II · device

Product

Bioseal Trachea Extender 1/pl 50pk/Cs, REF TRAX01/50, LOT XXXX, STERILE EO, Single Use Only, Date of Manufacture XXXX, Expiration Date XXXX, LF, UDI: (01) 00630094916019 - Product Usage: Airway connectors intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or mask.

Reason for recall

The reported stress crack in the port of the swivel elbow where the flip cap is inserted could result in leakage from the breathing system resulting in the prescribed ventilation not being delivered to the patient. These cracks could possibly leak if they reach a significant size and pose a serious heath risk to patient.

Distribution

US Nationwide distribution including in the state of CA.

Key facts

Status
Terminated
Initiation date
2019-08-15
Report date
2020-08-19
Termination date
2021-03-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Placentia, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2795-2020