Lina Librata recall in Canada: labelling and packaging issue
In plain language
This recall involves the Lina Librata Endometrial Ablation Device. It's being recalled because of an issue with an obsolete quick reference guide. This guide led to incorrect interpretation of device alarms and patient injury. This recall applies to the quick reference guide only.
What to do
- Contact the manufacturer for more information.
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Affected products
Lina Librata, Endometrial Ablation Device
Model: LIB-1
Lot: (01)05708265013487
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: (01)05708265013487
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: LIB-1
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?
This recall involves the Lina Librata Endometrial Ablation Device. It's being recalled because of an issue with an obsolete quick reference guide. This guide led to incorrect interpretation of device alarms and patient injury. This recall applies to the quick reference guide only.
What should consumers do?
Contact the manufacturer for more 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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on February 7, 2023.
Is the Lina Medical Aps brand affected by this recall?
Yes, Lina Medical Aps products are affected by this recall. This recall involves the Lina Librata Endometrial Ablation Device. It's being recalled because of an issue with an obsolete quick reference guide. This guide led to incorrect interpretation of device alarms and patient injury. This recall applies to the quick reference guide only.