Medline Anesthesia Pediatric Circuit 7: 10mm Tubing Disconnect Hazard
Medline recalls pediatric anesthesia circuits with disconnected 10mm tubing that could cause breathing issues during surgery.
Use caution until it’s fixed
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Contact the company
What happened, in plain English
Medline is recalling pediatric anesthesia circuits that have a disconnected 10mm green inspiratory tubing. This could lead to breathing problems during surgery if the circuit is used without fixing the issue. Read more at govinfonow.com/recall/66590-medline-anesthesia-pediatric-circuit-7-10mm-tubing-disconnect-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/66590-medline-anesthesia-pediatric-circuit-7-10mm-tubing-disconnect-hazard · Updated September 23, 2026 · FDA enforcement record: FDA #Z-0698-2020
Cite this page
“Medline Anesthesia Pediatric Circuit 7: 10mm Tubing Disconnect Hazard.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/66590-medline-anesthesia-pediatric-circuit-7-10mm-tubing-disconnect-hazard. Based on FDA recall #Z-0698-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0698-2020%22&limit=1).
Why it’s dangerous
The 10mm green inspiratory tubing is disconnected from the tee connector at the machine end. This could cause the circuit to fail during surgery, leading to breathing problems for the patient.
Who’s affected
Healthcare providers using the specific pediatric anesthesia circuits with model DYNJAPF6057A and lots 19GBI659 or 19HBP065 are most at risk. This affects hospitals and clinics that use these circuits for children's anesthesia.
How to tell if you have this one
Check for the model number DYNJAPF6057A on the circuit. The product was sold with lots 19GBI659 and 19HBP065. This circuit is used for pediatric anesthesia in medical settings.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Circuit Connection
Inspect the 10mm green inspiratory tubing to ensure it is securely connected to the tee connector at the machine end.
Where it went and when
Where it was distributed
Distributed in Pennsylvania.
FDA distribution: “USA - 2 consignees in PA only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Pennsylvania.
Recall timeline
FDA published this recall 56 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0698-2020 (October 30, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0698-2020 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.