Epix Grasper recall in Canada: tissue damage risk
In plain language
This recall involves specific lot numbers of the Epix Grasper, C4130 and C4140, and procedural packs containing these models, sold in Canada. It's being recalled because a protruding rivet could cause tissue damage. This is a medical device recall for healthcare professionals and hospitals.
What to do
- Stop using the product immediately.
- Check the lot numbers if provided.
- Follow the return or disposal steps in the official notice.
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Affected products
Epix Grasper
Model: C4130, C4140
Lot: 1364578, 1371262, 1373260
K0880 laparoscopic cholecystectomy kit
K2887 clip applier kit
Why this matters
Tissue damage
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: 1364578, 1371262, 1373260
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: C4130, C4140
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?
Tissue damage
What should consumers do?
Stop using the product immediately. Check the lot numbers if provided. Follow the return or disposal steps in the official notice.
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. Tissue damage
When was this product recalled?
This product was recalled on April 17, 2020.
Is the Epix brand affected by this recall?
Yes, Epix products are affected by this recall. This recall involves specific lot numbers of the Epix Grasper, C4130 and C4140, and procedural packs containing these models, sold in Canada. It's being recalled because a protruding rivet could cause tissue damage. This is a medical device recall for healthcare professionals and hospitals.