Barbed sutures recall in Canada: Small bowel obstruction risk
In plain language
This recall involves V-LOC 180 Wound Closure Devices, Quill Knotless Tissue-Closure Devices, and Stratafix Spiral Knotless Tissue Control Devices sold in Canada. They are being recalled because they may cause small bowel obstruction. If you have had surgery using these devices and experience symptoms, contact your healthcare professional.
What to do
- Contact your healthcare professional if you have symptoms of small bowel obstruction after surgery.
- Symptoms include vomiting, abdominal pain, and inability to pass gas or stool.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Small bowel obstruction risk
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Small bowel obstruction risk
What should consumers do?
Contact your healthcare professional if you have symptoms of small bowel obstruction after surgery. Symptoms include vomiting, abdominal pain, and inability to pass gas or stool.
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. Small bowel obstruction risk
When was this product recalled?
This product was recalled on May 31, 2018.