FDA recall Z-0698-2020

Medline Industries Inc · Class II · device

Product

Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A

Reason for recall

The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.

Distribution

USA - 2 consignees in PA only

Key facts

Status
Ongoing
Initiation date
2019-10-30
Report date
2019-12-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Northfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0698-2020