International safety notice
Theradiag SA
United Kingdom / MHRA · GBR · Jul 20, 2021
Key facts
| Title | Theradiag SA |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | I-Tracker Infliximab |
| Manufacturer | Theradiag SA |
| Models | 002-100, 00055, 8.801.735, CT-P13, 146367, 002–100, F-77435, 20-30, 2120Z, 77183, 90136 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Jul 20, 2021 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes 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