Class II — Gf Health Products
| Recalling firm | GF Health Products, Inc. |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The front casters on the 6810A Lumex Drop Arm Versamode are incorrect. |
| Product | Drop Arm Versamode" |
| Quantity | 66 units |
| Distribution | Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada. |
| Initiated | 2021-03-24 |
| Classified | 2021-04-05 |
| Terminated | 2023-05-01 |
| Recall number | Z-1353-2021 |
| 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 — Gf Health Products (Z-1353-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/87606/
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