International safety notice
Kit Freelite® lambda libre humano (para uso en SPAPLUS®)
Spain / AEMPS · ESP · Oct 29, 2021
Key facts
| Title | Kit Freelite® lambda libre humano (para uso en SPAPLUS®) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit Freelite® lambda libre humano (para uso en SPAPLUS®) |
| Manufacturer | The Binding Site Group Limited, Reino Unido |
| Models | STD-6, LK018.L.S, 435251, 08038, 110.45-173.76, 472664, 91.822.52.89, 472776, 28022, 05051700012201, 05051700017145, LK018.S and 16 more |
| Event type | Safety Notice |
| Date | Oct 29, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 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