Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments Recalled by Teleflex Medical Due to For some of the recalled products, the security...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teleflex Medical directly.
Affected Products
Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue during laparoscopic surgery.
Quantity: 20,039 Total (US and OUS)
Why Was This Recalled?
For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
Where Was This Sold?
This product was distributed to 29 states: AL, AZ, CA, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MN, MO, NJ, NY, NC, OH, OR, PA, SC, TN, TX, UT, VA, WA, WV, WI
About Teleflex Medical
Teleflex Medical has 204 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report