International safety notice
CellPath
United Kingdom / MHRA · GBR · Jul 16, 2017
Key facts
| Title | CellPath |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | General Histology Instruments |
| Manufacturer | CellPath |
| Models | SAH-2222-03, MAE-IOOO-03P, CELLPATHO80, GP150901004, ZP160602053, PATHOLOGYSY16, OOO-03P, 50901004, 12434, 1831261, SAH-2222-03A |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Jul 16, 2017 |
| 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