International safety notice
T7 destornillador canulado AO (Asociación para el Estudio de la Osteosíntesis), referencia 110018531 y T7 destornillador sólido AO, referencia 110018541.
Spain / AEMPS · ESP · Apr 16, 2019
Key facts
| Title | T7 destornillador canulado AO (Asociación para el Estudio de la Osteosíntesis), referencia 110018531 y T7 destornillador sólido AO, referencia 110018541. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | T7 destornillador canulado AO (Asociación para el Estudio de la Osteosíntesis), referencia 110018531 y T7 destornillador sólido AO, referencia 110018541. |
| Manufacturer | Biomet Orthopaedics, Estados Unidos. |
| Models | PRODUCTOT7, 2019-00046, ZFA2019-00046», 110018541, 110018531Y, 91.822.52.89, 51758, 110018531, 2.12-1, 08038, 08040, 28022 and 1 more |
| Event type | Safety Notice |
| Date | Apr 16, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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