International safety notice
Dispositivos e instrumentos del sistema de sustitución femoral segmentario Compress: Ref.178350, Ref.178353, Ref.178356, Ref.178359, Ref.178537, Ref.178541, Ref.178545, Ref.178544, Ref.178738, Ref.178542, Ref.32-481123
Spain / AEMPS · ESP · Nov 23, 2018
Key facts
| Title | Dispositivos e instrumentos del sistema de sustitución femoral segmentario Compress: Ref.178350, Ref.178353, Ref.178356, Ref.178359, Ref.178537, Ref.178541, Ref.178545, Ref.178544, Ref.178738, Ref.178542, Ref.32-481123 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Dispositivos e instrumentos del sistema de sustitución femoral segmentario Compress: Ref.178350, Ref.178353, Ref.178356, Ref.178359, Ref.178537, Ref.178541, Ref.178545, Ref.178544, Ref.178738, Ref.178542, Ref.32-481123 |
| Manufacturer | Biomet Orthopaedics, 46582 Warsaw (Indiana), Estados Unidos |
| Models | 2018-601, 12–14, 48640, 178359, 91.822.52.89, ZFA2018-00446, 178353, REF.178537, REF.178350, 08110, REF.178738, REF.32-481123 and 56 more |
| Event type | Safety Notice |
| Date | Nov 23, 2018 |
At a glance
- No Recall
- Yes Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1