International safety notice
Randox Laboratories
United Kingdom / MHRA · GBR · Sep 23, 2019
Key facts
| Title | Randox Laboratories |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | NEFA |
| Manufacturer | Randox Laboratories |
| Models | 05055273203066, 485343, FA115, REC422 |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Sep 23, 2019 |
| Regulator page | gov.uk |
At a glance
- Yes 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