Integra Cranial Kit recall in Canada: Sterility concern
In plain language
This recall involves the Integra Cranial Kit sold in Canada. It's being recalled because the sterile packaging may have defects, creating a potential sterility concern. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
Cranial Kit - No Drugs
Model: INS-5HND
Lot: 7275713, 7289690
Why this matters
Sterility concern
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: 7275713, 7289690
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: INS-5HND
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?
Sterility concern
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. Sterility concern
When was this product recalled?
This product was recalled on May 8, 2024.
Is the Integra Pain Management brand affected by this recall?
Yes, Integra Pain Management products are affected by this recall. This recall involves the Integra Cranial Kit sold in Canada. It's being recalled because the sterile packaging may have defects, creating a potential sterility concern. Healthcare professionals should contact the manufacturer for more information.