FDA recall Z-0313-2022
Howmedica Osteonics Corp. · Class II · device
Product
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
Reason for recall
XXX
Distribution
Puerto Rico
Key facts
- Status
- Ongoing
- Initiation date
- 2021-10-15
- Report date
- 2021-12-08
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Mahwah, NJ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0313-2022