CLASS II ONGOING Device recall · Reported 25 Dec 2019 · FDA Enforcement Report
Anesthesia Pediatric Circuit 72" recalled by Medline Industries
Medline Industries is recalling Anesthesia Pediatric Circuit 72", distributed in Pennsylvania. The recall was initiated on 30 Oct 2019 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-0698-2020
- FDA event ID
- 84283
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 30 Oct 2019
- FDA classified
- 18 Dec 2019
- Reported
- 25 Dec 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 30 Oct 2019 | Recall initiated by company | |
| 18 Dec 2019 | Classified by FDA | +49 days |
| 25 Dec 2019 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Product as listed by the FDA
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
Where it was distributed
USA - 2 consignees in PA only
Questions about this recall
Why was it recalled?
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Which lots are affected?
Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065
Where was it sold?
USA - 2 consignees in PA only
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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