Class II — Zyno Medical LLC
| Recalling firm | Zyno Medical LLC. |
|---|---|
| Registered facility | Zyno Medical LLC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps have faulty power supply modules that will not provide a charge to the rechargeable battery within the pump. This may lead to the battery having insufficient or no charge available to the pump when it is unplugged from the AC mains power. |
| Product | Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion Pumps |
| Quantity | 88 units |
| Distribution | US Nationwide distribution. |
| Initiated | 2024-06-04 |
| Classified | 2024-07-03 |
| Recall number | Z-2263-2024 |
| 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 — Zyno Medical LLC (Z-2263-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94768/
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