Anesthesia Pediatric Circuit 72" — Class II medical device recall Z-0698-2020
Ongoing recall by Medline Industries Inc, reported 2019-12-25. The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circu
| Recall number | Z-0698-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2019-10-30 |
| Classified | 2019-12-18 |
| Reported by FDA | 2019-12-25 |
| Quantity | 4,040 units |
| Lot numbers | 19GBI659, 19HBP065 |
| Model numbers | DYNJAPF6057A |
Product
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
Reason for recall
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0698-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.