HIGH
Brand hub
Howmedica Osteonics Recalls
4 recalls found for Howmedica Osteonics. Check current safety alerts and related brands before using affected products.
- Active recalls
- 4
- Pages
- 1
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Stryker Recalls CranialMask Tracker Due to Device Error
When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.
Howmedica Osteonics
When the
Health & Personal Care
HIGH
FDA DEVICE
Howmedica Osteonics Recalls 55 EXETER V40 Surgical Stems Due to Product Mix Risk
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.
Howmedica Osteonics
a potential
Brand Statistics
Total Recalls
4
Pages
1