International safety notice
DiaClon Rh-Subgroups + K
Swiss / SwissMedic · CHE · Jun 13, 2019
Key facts
| Title | DiaClon Rh-Subgroups + K |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | DiaClon Rh-Subgroups + K |
| Manufacturer | DiaMed GmbH |
| Models | 001398, 002126, 50710, Rond23, I001398, I002126, 50130, I002127, 002124, 50110, 002127, 002125 and 4 more |
| Event type | Safety Notice |
| Date | Jun 13, 2019 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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