FDA Medical Device Recalls (openFDA)
Medline Industries Inc: Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
- Recall number
- Z-0698-2020
- Recalling firm
- Medline Industries Inc
- Product
- Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
- Status
- Open, Classified
- Initiated
- 2019-10-30
- Posted
- not on file
- Terminated
- not on file
- Reason
- The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
- Root cause
- Under Investigation by firm
- Action
- Consignees were notified via email by their sales representative on 11/05/2019. A letter with response form was sent via email to each consignee. Responses will be recorded and subsequent letters will be sent to those consignees that do not respond in the allotted time.
- Quantity
- 4040 units
- Distribution
- USA - 2 consignees in PA only
- Lot, serial or model codes
- Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- CAI
- Firm FEI
- 1417592
- Firm city
- Northfield
- Firm state
- IL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28