International safety notice
Sustituto óseo de hidroxilapatita inyectable HydroSet, modelo 397010
Spain / AEMPS · ESP · Oct 11, 2018
Key facts
| Title | Sustituto óseo de hidroxilapatita inyectable HydroSet, modelo 397010 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sustituto óseo de hidroxilapatita inyectable HydroSet, modelo 397010 |
| Manufacturer | Stryker Leibinger GmbH & Co. KG, Alemania |
| Models | 2018-518, 397010, 28108, 28022, CG5ZKJ35DD, 2.12-1, 79111, 47863, LOTEIC02608, 1875982, IC02617, RA2018-1875982 and 3 more |
| Event type | Safety Notice |
| Date | Oct 11, 2018 |
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