International safety notice
Optisure Dual Coil Defibrillation lead
Swiss / SwissMedic · CHE · Nov 16, 2015
Key facts
| Title | Optisure Dual Coil Defibrillation lead |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | Optisure Dual Coil Defibrillation lead |
| Manufacturer | St. Jude Medical |
| Models | 55117, LDA220Q, LDA220, LDP220Q, 607471 |
| Event type | Safety Notice |
| Date | Nov 16, 2015 |
| Regulator page | fsca.swissmedic.ch |
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