Fetal Spiral Electrode recall in Canada: spiral tip may break off
In plain language
This recall involves PHILIPS MEDICAL SYSTEMS Fetal Spiral Electrodes sold in Canada. It's being recalled because the spiral tip may break off during use, potentially requiring surgery to remove it. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Fetal Spiral Electrode
Model: 9898 031 37631
Lot: Not applicable.
Why this matters
Requires surgical intervention
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: 9898 031 37631
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?
Requires surgical intervention
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. Requires surgical intervention
When was this product recalled?
This product was recalled on December 15, 2022.
Is the PHILIPS MEDICAL SYSTEMS brand affected by this recall?
Yes, PHILIPS MEDICAL SYSTEMS products are affected by this recall. This recall involves PHILIPS MEDICAL SYSTEMS Fetal Spiral Electrodes sold in Canada. It's being recalled because the spiral tip may break off during use, potentially requiring surgery to remove it. Healthcare professionals should contact the manufacturer for more information.