FDA recall Z-1727-2019

Stryker Corporation · Class II · device

Product

Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP), REF 0620-040-680, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

Reason for recall

The heated tube sets were consistently leaking and detaching from the cassette.

Distribution

Distribution was nationwide to medical facilities. There was government/military distribution. Foreign distribution was made to Argentina, Brazil, Canada, Chile, Colombia, (EMEA-no specific address/country listed), India, Japan, Latin America (no country listed), Mexico, Saudi Arabia, UAE, and Uruguay.

Key facts

Status
Terminated
Initiation date
2019-03-07
Report date
2019-06-12
Termination date
2024-03-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Jose, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1727-2019