Defigard Touch7 Monitor And Defibrillator recall in Canada: performance issue
In plain language
This recall involves the Defigard Touch7 Monitor And Defibrillator sold in Canada. It's being recalled because a performance issue could lead to inoperative defibrillation. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Defigard Touch7 Monitor And Defibrillator
Model: 1-128-9900
Lot: All lots
Why this matters
Inoperative defibrillation
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: 1-128-9900
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?
Inoperative defibrillation
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. Inoperative defibrillation
When was this product recalled?
This product was recalled on November 23, 2023.
Is the Schiller Medical brand affected by this recall?
Yes, Schiller Medical products are affected by this recall. This recall involves the Defigard Touch7 Monitor And Defibrillator sold in Canada. It's being recalled because a performance issue could lead to inoperative defibrillation. Stop using the product and follow the return/repair steps in the official notice.