COMPANION 1000 PORTABLE recall in Canada: potential injury risk
In plain language
This recall involves the COMPANION 1000 PORTABLE medical device sold in Canada. It's being recalled because it could cause injury to patients when used at 6 LPM for an extended time. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model and serial numbers.
- Return, repair, or dispose of it as instructed.
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Affected products
COMPANION 1000 PORTABLE
Model: B-775099-00
Lot: 85010101 to 89011701
Why this matters
Potential injury 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: 85010101 to 89011701
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: B-775099-00
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?
Potential injury risk
What should consumers do?
Stop using the product immediately. Check the model and serial numbers. Return, repair, or dispose of it as instructed.
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. Potential injury risk
When was this product recalled?
This product was recalled on October 30, 2020.