Perseus A500 recall in Canada: Device performance issue
In plain language
This recall involves the Perseus A500 medical device sold in Canada. It's being recalled because the internal backup battery may fail, causing unexpected shutdown. This recall is for healthcare professionals.
What to do
- Contact the manufacturer for additional information.
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Affected products
Perseus A500
Model: MK06000
Lot: All lots
Why this matters
Device 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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: MK06000
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?
Device performance issue
What should consumers do?
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. Device performance issue
When was this product recalled?
This product was recalled on March 14, 2024.
Is the Draegerwerk Ag & Co. Kgaa brand affected by this recall?
Yes, Draegerwerk Ag & Co. Kgaa products are affected by this recall. This recall involves the Perseus A500 medical device sold in Canada. It's being recalled because the internal backup battery may fail, causing unexpected shutdown. This recall is for healthcare professionals.