Zyno Medical Z800 — Class II medical device recall Z-2263-2024
Ongoing recall by Zyno Medical LLC, reported 2024-07-10, distributed nationwide. Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps have faulty power supply modules that
| Recall number | Z-2263-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zyno Medical LLC, Natick, MA, United States |
| Recall initiated | 2024-06-04 |
| Classified | 2024-07-03 |
| Reported by FDA | 2024-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 88 units |
| UPC / GTIN / UDI-DI | 00814371020013, 00814371020020, 00814371020037 |
| Serial numbers | 500010, 500054, 500066, 501954, 502832, 503770, 503950, 504296, 504496, 601191, 601424, 601438, 601782, 601905, 602023, 602280, 602518, 602521, 603096, 603717, 604135, 604576, 605032, 605090, 607171 and 67 more |
Product
Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion Pumps
Reason for recall
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.
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-2263-2024. 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.