International safety notice
Inserto polietileno para artroplastia de cadera.; Inserto para artroplastia de rodilla K-MOD.
Spain / AEMPS · ESP · May 19, 2021
Key facts
| Title | Inserto polietileno para artroplastia de cadera.; Inserto para artroplastia de rodilla K-MOD. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Inserto polietileno para artroplastia de cadera.; Inserto para artroplastia de rodilla K-MOD. |
| Manufacturer | Gruppo Bioimpianti S.r.L, Italia. |
| Models | 20068, 120701815, 00390251650393, 306096, 120700742, 10450142, 120700733, AG0475, 2021-277, 120700745, AG0344, 18.03.2021 and 26 more |
| Event type | Safety Notice |
| Date | May 19, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 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