International safety notice
GELITA SPON, GELITA ENT devices FSN 1, GELITA SPON, GELITA ENT devices FSN 2
Ireland / HPRA · IRL · Aug 3, 2022
Key facts
| Title | GELITA SPON, GELITA ENT devices FSN 1, GELITA SPON, GELITA ENT devices FSN 2 |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | GELITA SPON, GELITA ENT devices FSN 1 GELITA SPON, GELITA ENT devices FSN 2 |
| Manufacturer | Gelita Medical GmbH |
| Models | 4260293130112, RAPID³, 4260293133199, 4260293130723, GE-6385, 4260293130082, GS-004, 4260293133052, 4260293130730, 4260293137777, GMED_FSN_JULY2022, 4260293137050 and 98 more |
| Event type | Recall |
| Date | Aug 3, 2022 |
At a glance
- Yes Recall
- No Field safety notice
- 1–9 Matching device models 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