Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to Customer reports of the device handset continuing to...
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 COVIDIEN MEDTRONIC directly.
Affected Products
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.
Quantity: 24,703 Units
Why Was This Recalled?
Customer reports of the device handset continuing to operate after release of the activation button.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About COVIDIEN MEDTRONIC
COVIDIEN MEDTRONIC has 55 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report