International safety notice
Optipac 40 Refobacin Revision and Optipac 80 Refobacin Revision
Ireland / HPRA · IRL · Jan 3, 2018
Key facts
| Title | Optipac 40 Refobacin Revision and Optipac 80 Refobacin Revision |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Optipac 40 Refobacin Revision and Optipac 80 Refobacin Revision |
| Manufacturer | Biomet Orthopedics Switzerland GmbH |
| Models | 4730501163-1, 4732501165-1, 2017-500, A722B08910, A620A01788, A705B05130, A722B00240, B705B05128, REV.2, A705B06130, A620A0178A, A648C04670 and 4 more |
| Event type | Recall |
| Date | Jan 3, 2018 |
| Regulator page | hpra.ie |
At a glance
- Yes Recall
- No Field safety notice
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