Valon Fetal Monitor - Risk Of Inaccurate Ultrasound-derived Fetal Heart Rate Monitoring
Avalon Fetal Monitor Recall Philips is recalling Avalon fetal monitors across Canada because they may display inaccurate fetal heart rate readings when using ultrasound monitoring. The inaccuracy could result from software issues that affect how the device processes and displays heart rate data. This recall affects healthcare facilities and clinics using this fetal monitoring equipment.
- Reason
- Product safety
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DRUGS
- Recall date
- 2019-10-09
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DRUGS
Recall details on Nibble Recalls: https://trynibble.app/recalls/ef4e9672-a5b2-4d40-8002-df32a9a62a62