International safety notice
Baxter
United Kingdom / MHRA · GBR · Jan 8, 2021
Key facts
| Title | Baxter |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Cartridge Single Needle, Artiset HD DNL HC, Artiset Prepost, Cartridge with Hemoscan, Artiset HD SN HC, Cartridge Extended Patient Lines, Cartridge Ext/ Patient Lines + Infusion, Cartridge Standard, Cartridge Low Weight, Cartridge Low Weight Low Volume, Physioset HD DNL HC, Physioset Prepost |
| Manufacturer | Baxter |
| Models | 955075, 01604, 206034, FA-2020-068, 01635, 955077, 114533 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Jan 8, 2021 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes 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