FDA Device recall Z-1353-2021
Drop Arm Versamode"
- FDA Device
- Class II
- terminated
- Published 2021-04-14
On 2021-04-14 the FDA classified a Class II recall of Drop Arm Versamode" by Gf Health Products, citing the front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1353-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-03-24 |
| Published | 2021-04-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Gf Health Products |
| Distribution | US |
Product
Drop Arm Versamode"
Reason
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Identifiers
| code_info | Model: 6810A; Device Identifier: M36868101; and Lot number: BMW316BS |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1353-2021%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.