RENASYS™ EDGE Negative Pressure Wound Therapy
In plain language
This recall involves RENASYS™ EDGE Negative Pressure Wound Therapy devices sold in Canada. They are being recalled because the battery may not recharge if not maintained properly. The device will still work on mains power.
What to do
- Contact the manufacturer for more information.
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Affected products
RENASYS™ EDGE Negative Pressure Wound Therapy
Model: 66803126
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Performance issue
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 66803126
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
What should consumers do?
Contact the manufacturer for more 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
When was this product recalled?
This product was recalled on October 23, 2024.
Is the Smith & Nephew Medical Ltd. brand affected by this recall?
Yes, Smith & Nephew Medical Ltd. products are affected by this recall. This recall involves RENASYS™ EDGE Negative Pressure Wound Therapy devices sold in Canada. They are being recalled because the battery may not recharge if not maintained properly. The device will still work on mains power.