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