Class II — Medline Industries Inc
| Recalling firm | Medline Industries, LP |
|---|---|
| Registered facility | View this company's 31 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit. |
| Product | Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A |
| Quantity | 4040 units |
| Distribution | USA - 2 consignees in PA only |
| Initiated | 2019-10-30 |
| Classified | 2019-12-18 |
| Recall number | Z-0698-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medline Industries Inc (Z-0698-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/84283/
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