MED-RX® Epidural Anesthesia Kit recall in Canada: Performance issue
In plain language
This recall involves the MED-RX® Epidural Anesthesia Kit sold in Canada. It's being recalled because the depth markers on the epidural catheter may fade or wear away during use. This could delay medical procedures and require product replacement. This recall is intended for healthcare professionals.
What to do
- Contact the manufacturer, Canadian Hospital Specialties Ltd., for additional information.
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Affected products
MED-RX® Epidural Anesthesia Kit
Model: 80-8169
Lot: 191306
Why this matters
Performance issue with medical device
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: 191306
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 80-8169
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?
Performance issue with medical device
What should consumers do?
Contact the manufacturer, Canadian Hospital Specialties Ltd., for 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. Performance issue with medical device
When was this product recalled?
This product was recalled on May 9, 2024.
Is the MED-RX® brand affected by this recall?
Yes, MED-RX® products are affected by this recall. This recall involves the MED-RX® Epidural Anesthesia Kit sold in Canada. It's being recalled because the depth markers on the epidural catheter may fade or wear away during use. This could delay medical procedures and require product replacement. This recall is intended for healthcare professionals.