Arjo Portable Scale Adaptor recall in Canada: fall risk
In plain language
This recall involves the Arjo Portable Scale Adaptor sold in Canada. It's being recalled because the strap could detach during patient transfer, which may lead to a fall. Contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Arjo Portable Scale Adaptor
Model: 700.05725
Lot: Lots produced between Sep-13-2021 to Nov 10-2022
Why this matters
Fall risk, potential for major trauma/head injury
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: Lots produced between Sep-13-2021 to Nov 10-2022
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 700.05725
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?
Fall risk, potential for major trauma/head injury
What should consumers do?
Stop using the product immediately. Contact the manufacturer 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. Fall risk, potential for major trauma/head injury
When was this product recalled?
This product was recalled on March 22, 2023.
Is the Arjohuntleigh Ab brand affected by this recall?
Yes, Arjohuntleigh Ab products are affected by this recall. This recall involves the Arjo Portable Scale Adaptor sold in Canada. It's being recalled because the strap could detach during patient transfer, which may lead to a fall. Contact the manufacturer for more information.