FDA recall Z-1941-2020
Medtronic Sofamor Danek USA Inc · Class II · device
Product
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Reason for recall
Nonconforming product; length of the product measured shorter than the labeled length.
Distribution
US Nationwide distribution in the states of CA and MI.
Key facts
- Status
- Terminated
- Initiation date
- 2020-03-26
- Report date
- 2020-05-20
- Termination date
- 2021-03-26
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Memphis, TN, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1941-2020