Z-0698-2020 Class II Ongoing
FDA device recall Z-0698-2020 was initiated by Medline Industries Inc on October 30, 2019 and is designated Class II. Reason for recall: The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit. The recall status is ongoing. Affected quantity: 4040 units.
Recall Details
- Product Type
- Devices
- Report Date
- December 25, 2019
- Initiation Date
- October 30, 2019
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4040 units
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.
Distribution Pattern
USA - 2 consignees in PA only
Code Information
Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065