Drop Arm Versamode" — Class II medical device recall Z-1353-2021
Terminated recall by Gf Health Products, reported 2021-04-14, distributed nationwide. The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
| Recall number | Z-1353-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Gf Health Products, Atlanta, GA, United States |
| Recall initiated | 2021-03-24 |
| Classified | 2021-04-05 |
| Reported by FDA | 2021-04-14 |
| Terminated | 2023-05-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Quantity | 66 units |
| Lot numbers | BMW316BS |
| Model numbers | 6810A |
Product
Drop Arm Versamode"
Reason for recall
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
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-1353-2021. 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.