FDA recall Z-1353-2021
Gf Health Products · Class II · device
Product
Drop Arm Versamode"
Reason for recall
The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Distribution
Distributed nationwide to CA, WI, PA, IL, and TX. Distributed internationally to Mexico and Canada.
Key facts
- Status
- Terminated
- Initiation date
- 2021-03-24
- Report date
- 2021-04-14
- Termination date
- 2023-05-01
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Atlanta, GA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1353-2021