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Devices
Device Recall Zweimueller Type Stem SCS
Model / Serial
Part No. 120.00.15 120.00.00 120.00.01 120.00.02 120.00.03 120.00.04 120.00.05 120.00.06 120.00.07 120.00.08 120.00.09 120.00.10 123.00.03 123.00.04 123.00.05 123.00.06 123.00.07 123.00.08 123.00.09 126.00.03 126.00.04 126.00.05 126.00.06 126.00.07 126.00.08 126.00.09 126.00.10 126.00.11
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution including the states of CA, MD, TX, NV, and WI.
Product Description
Zweimueller Type Stem SCS-Standard Sz 01 || Zweimueller Type Stem SCS-Standard Sz 00 || Zweimueller Type Stem SCS-Standard Sz 1 || Zweimueller Type Stem SCS-Standard Sz 2 || Zweimueller Type Stem SCS-Standard Sz 3 || Zweimueller Type Stem SCS-Standard Sz 4 || Zweimueller Type Stem SCS-Standard Sz 5 || Zweimueller Type Stem SCS-Standard Sz 6 || Zweimueller Type Stem SCS-Standard Sz 7 || Zweimueller Type Stem SCS-Standard Sz 8 || Zweimueller Type Stem SCS-Standard Sz 9 || Zweimueller Type Stem SCS-Standard Sz 10 || Zweimueller Type Stem SCL-Lateralized Sz 3 || Zweimueller Type Stem SCL-Lateralized Sz 4 || Zweimueller Type Stem SCL-Lateralized Sz 5 || Zweimueller Type Stem SCL-Lateralized Sz 6 || Zweimueller Type Stem SCL-Lateralized Sz 7 || Zweimueller Type Stem SCL-Lateralized Sz 8 || Zweimueller Type Stem SCL-Lateralized Sz 9 || Zweimueller Type Stem SCR-Revision Sz 3 || Zweimueller Type Stem SCR-Revision Sz 4 || Zweimueller Type Stem SCR-Revision Sz 5 || Zweimueller Type Stem SCR-Revision Sz 6 || Zweimueller Type Stem SCR-Revision Sz 7 || Zweimueller Type Stem SCR-Revision Sz 8 || Zweimueller Type Stem SCR-Revision Sz 9 || Zweimueller Type Stem SCR-Revision Sz 10 || Zweimueller Type Stem SCR-Revision Sz 11 || Variety of hip and knee implants and instruments, multiple uses.
Manufacturer
Orthopedic Alliance LLC
1 Event
Recall of Device Recall Zweimueller Type Stem SCS
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Manufacturer
Orthopedic Alliance LLC
Manufacturer Address
Orthopedic Alliance LLC, 26157 Jefferson Ave, Murrieta CA 92562-9561
Source
USFDA
Language
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