Recall Z-0698-2020— Medline Industries Inc
Class II · Ongoing
Class II FDA medical device recall by Medline Industries Inc, initiated 2019-10-30. FDA's recall record names no specific 510(k) clearance for this event. Product: Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A. Reason: The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit..
- Recalling firm
- Medline Industries Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2019-10-30
- Firm location
- Northfield, IL, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.