FDA Device recall Z-1865-2025
Z-800 Infusion System
- FDA Device
- Class I
- ongoing
- Published 2025-06-18
On 2025-06-18 the FDA classified a Class I recall of Z-800 Infusion System by Zyno Medical, citing unreleased software versions were installed on distributed devices without verification or validation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1865-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-05-07 |
| Published | 2025-06-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Zyno Medical |
| Distribution | US |
Product
Z-800 Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Reason
Unreleased software versions were installed on distributed devices without verification or validation.
Identifiers
| code_info | Lot Code: Model Number; Z800; UDI-DI: 00814377102006; Serial No.: 800242; 801925; 802867; 900875; 901058; 901089; 90110…Lot Code: Model Number; Z800; UDI-DI: 00814377102006; Serial No.: 800242; 801925; 802867; 900875; 901058; 901089; 901101; 901126; 901143; 901567; 904021; 904073; 800378; 801950; 803020; 900914; 901061; 901090; 901102; 901129; 901145; 901795; 904023; 904083; 801082; 802113; 803268; 900961; 901066; 901091; 901103; 901130; 901230; 904004; 904026; 904087; 801353; 802131; 803526; 900964; 901070; 901092; 901110; 901131; 901240; 904006; 904027; 904093; 801420; 802160; 803768; 901001; 901076; 901093; 901112; 901132; 901241; 904007; 904028; 904094; 801503; 802645; 900029; 901014; 901077; 901094; 901113; 901133; 901244; 904009; 904029; 905077; 801601; 802753; 900035; 901024; 901081; 901095; 901115; 901134; 901245; 904011; 904030; 905162; 801640; 802764; 900051; 901041; 901083; 901096; 901116; 901136; 901246; 904012; 904031; 906681; 801852; 802771; 900115; 901054; 901085; 901097; 901117; 901138; 901249; 904013; 904038; 906692; 801855; 802774; 900133; 901055; 901086; 901098; 901118; 901140; 901250 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1865-2025%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.