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Open, Classified

Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A

FDA Recall Z-0698-2020 · Posted None

Recalling FirmMedline Industries Inc
Recall StatusOpen, Classified
Product CodeCAI
Date Initiated2019-10-30
Product Quantity4040 units

Reason for Recall

The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.

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.

Root Cause

Under Investigation by firm

Distribution Pattern

USA - 2 consignees in PA only

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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