Detachable Endo Pocket recall in Canada: Performance issue
In plain language
This recall involves the Detachable Endo Pocket, a medical device used in surgical procedures. It's being recalled because a tube inside the pouch may stretch out, potentially delaying surgery if it falls into the surgical site. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer, Conmed Corporation, if you require additional information.
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Affected products
Detachable Endo Pocket
Model: SB936-CA, SB979-CA
Lot: 6252207201, 6252212124, 6252212017, 6252209205
Why this matters
Performance issue
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: 6252207201, 6252212124, 6252212017, 6252209205
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: SB936-CA, SB979-CA
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
What should consumers do?
Contact the manufacturer, Conmed Corporation, if you require 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
When was this product recalled?
This product was recalled on July 31, 2024.
Is the Conmed Corporation brand affected by this recall?
Yes, Conmed Corporation products are affected by this recall. This recall involves the Detachable Endo Pocket, a medical device used in surgical procedures. It's being recalled because a tube inside the pouch may stretch out, potentially delaying surgery if it falls into the surgical site. Healthcare professionals should contact the manufacturer for more information.