FDA recall Z-0256-2020
Centurion Medical Products Corporation · Class II · device
Product
PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
Reason for recall
Supplier initiated recall of the GRIPPER Needles
Distribution
IL
Key facts
- Status
- Terminated
- Initiation date
- 2019-07-15
- Report date
- 2019-11-06
- Termination date
- 2020-08-31
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Williamston, MI, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0256-2020