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Devices
Device Recall Femoral head
Model / Serial
Item No. 1201-1126 1201-1326 1201-1526 1201-1726 1201-1028 1201-1128 1201-1428 1201-1828 1201-1032 1201-1132 1201-1432 1201-1832 1201-1036 1201-1136 1201-1436 1201-1836
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
Femoral head, standard, ¿26mm, +0mm || Femoral head,medium, ¿26mm,+3mm || Femoral head, long, ¿26mm, +6mm || Femoral head, X-long, ¿26mm, +9mm || Femoral head, ¿28mm, -3mm || Femoral head, ¿28mm, +0mm || Femoral head, ¿28mm, +5mm || Femoral head, ¿28mm, +10mm || Femoral head, ¿32mm, -3mm || Femoral head, ¿32mm, +0mm || Femoral head, ¿32mm, +5mm || Femoral head, ¿32mm, +10mm || Femoral head, ¿36mm, -3mm || Femoral head, ¿36mm, +0mm || Femoral head, ¿36mm, +5mm || Femoral head, ¿36mm, +10mm || Variety of hip and knee implants and instruments, multiple uses.
Manufacturer
Orthopedic Alliance LLC
1 Event
Recall of Device Recall Femoral head
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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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