Avalon US Transducer recall in Canada: Inaccurate heart rate readings
In plain language
This recall involves Avalon US Transducers (model 867246) sold in Canada. It's being recalled because it may report inaccurate fetal heart rate measurements when monitoring multiples. Healthcare professionals should contact the manufacturer for additional information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Avalon US Transducer
Model: 867246
Lot: Not applicable
Why this matters
Inaccurate fetal heart rate readings
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: Not applicable
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 867246
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Inaccurate fetal heart rate readings
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Inaccurate fetal heart rate readings
When was this product recalled?
This product was recalled on March 12, 2025.
Is the Philips Medizin Systeme Boblingen Gmbh brand affected by this recall?
Yes, Philips Medizin Systeme Boblingen Gmbh products are affected by this recall. This recall involves Avalon US Transducers (model 867246) sold in Canada. It's being recalled because it may report inaccurate fetal heart rate measurements when monitoring multiples. Healthcare professionals should contact the manufacturer for additional information.