Vega505EE & SwiftHook recall in Canada: detachment risk
In plain language
This recall involves the Vega505EE and SwiftHook medical devices sold in Canada. They are being recalled because the SwiftHook may detach if not properly attached, which could lead to injury. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and serial numbers provided.
- Contact Handicare AB for instructions on return or repair.
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Affected products
Vega505EE
Model: 60600003
Lot: 60600003
SwiftHook
Model: 70200008
Lot: 70200008
Why this matters
Detachment risk
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: 60600003, 70200008
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 60600003, 70200008
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?
Detachment risk
What should consumers do?
Stop using the product immediately. Check the model and serial numbers provided. Contact Handicare AB for instructions on return or repair.
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. Detachment risk
When was this product recalled?
This product was recalled on September 8, 2020.