Medline Industries Inc Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
Brand
Medline Industries Inc
Lot Codes / Batch Numbers
Product Model DYNJAPF6057A, Lots 19GBI659 and 19HBP065
Products Sold
Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065
Medline Industries Inc is recalling Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A due to The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN, PA
Page updated: Jan 10, 2026