International safety notice
Perno de bloqueo, Tornillo de compresión y Cápsula del extremo, distribuidos a partir del 10 de marzo de 2020
Spain / AEMPS · ESP · May 19, 2020
Key facts
| Title | Perno de bloqueo, Tornillo de compresión y Cápsula del extremo, distribuidos a partir del 10 de marzo de 2020 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Perno de bloqueo, Tornillo de compresión y Cápsula del extremo, distribuidos a partir del 10 de marzo de 2020 |
| Manufacturer | Stryker Trauma GmbH, Alemania |
| Models | K0302FD, 18964032S, K037E2D, 18300015S, K030F1E, K029C39, K030F17, K030315, K030307, K0302F9, 18965030S, K0EAC03 and 71 more |
| Event type | Safety Notice |
| Date | May 19, 2020 |
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