International safety notice
Philips
United Kingdom / MHRA · GBR · Oct 18, 2022
Key facts
| Title | Philips |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | HeartStart Intrepid Monitor/Defibrillator |
| Manufacturer | Philips |
| Models | CN73905485, CN73905808, CN73905771, CN73905538, CN73905823, CN73905448, CN73905507, CN73905441, CN73905483, CN73905787, CN73905798, CN73905478 and 225 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Medical specialty | Anaesthetics, Cardiology, Care home staff, Cosmetic surgery, Critical care, Dentistry, Dispensing GP practices, General practice, General surgery, Haematology and oncology, Infection prevention, Obstetrics and gynaecology, Ophthalmology, Orthopaedics, Paediatrics, Pathology, Pharmacy, Physiotherapy and occupational therapy, Radiology, Renal medicine, Theatre practitioners, Urology, Vascular and cardiac surgery |
| Date | Oct 18, 2022 |
| 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