FDA Enforcement
Class II
Terminated
TIBIAL TRAY , SIZE 2, REF 90-SRK-200200, QTY: 1, STERILE R, total knee replacement .
Recall: Z-2635-2016
·
Reported August 31, 2016
Enforcement
- Recall Number
- Z-2635-2016
- Event ID
- 74850
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Medtronic Sofamor Danek USA Inc
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Report Date
- August 31, 2016
- Initiation Date
- July 18, 2016
- Classification Date
- August 23, 2016
- Termination Date
- November 22, 2016
- Address
- 1800 Pyramid Pl, Memphis, TN, 38132-1703, United States
Description
TIBIAL TRAY , SIZE 2, REF 90-SRK-200200, QTY: 1, STERILE R, total knee replacement .
Reason
The alpha total knee replacement components that may have not been passivated in accordance with the requirements of the job traveler.
Code Info
P239166, P239167,
Distribution
AR, MN,MA
Quantity
3 units