Kiestra ReadA recall in Canada: performance issue
In plain language
This recall involves the Kiestra ReadA, a medical device used in healthcare settings in Canada. It's being recalled because a performance issue can affect remote connectivity, leading to delays in plate retrieval. Healthcare facilities should contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
Kiestra ReadA
Model: 446948
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Performance issue leading to delays
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 446948
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?
Performance issue leading to delays
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. Performance issue leading to delays
When was this product recalled?
This product was recalled on February 18, 2026.
Is the Bd Kiestra B.V. brand affected by this recall?
Yes, Bd Kiestra B.V. products are affected by this recall. This recall involves the Kiestra ReadA, a medical device used in healthcare settings in Canada. It's being recalled because a performance issue can affect remote connectivity, leading to delays in plate retrieval. Healthcare facilities should contact the manufacturer for more information.