FDA Device recall Z-0698-2020
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
- FDA Device
- Class II
- ongoing
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class II recall of Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A by Medline Industries, citing the 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0698-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-10-30 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medline Industries |
| Distribution | PA |
Product
Anesthesia Pediatric Circuit 72", Model DYNJAPF6057A
Reason
The 10mm inner green inspiratory tubing is disconnected from the tee connector at the machine end of the circuit.
Identifiers
| code_info | Product Model DYNJAPF6057A; Lots 19GBI659 and 19HBP065 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
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FDA Device · Class II · 2026-10-21 · Medline Industries - Medline surgical convenience kits labeled as: 1) NEURO-SPINE BASIN PACK, Medline Product Number/SKU DYNJ80055A
FDA Device · Class II · 2026-10-21 · Medline Industries - Medline surgical convenience kits labeled as: 1) VEIN HARVESTING PACK-LF, Medline product number/SKU DYNJ0826732J
FDA Device · Class II · 2026-10-21 · Medline Industries - Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A &
FDA Device · Class II · 2026-10-21 · Medline Industries
All Medline Industries recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0698-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.