Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien ROTICULATOR 30-V3 Single Use Stapler REF# 017619 The RETICULA Recalled by Covidien LP Due to Potential for the sterility barrier to be compromised.
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 LP directly.
Affected Products
Covidien ROTICULATOR 30-V3 Single Use Stapler REF# 017619 The RETICULA TOR TM Single Use Staplers have applications in abdominal, gynecologic and pediatric surgery for resection, transection, and creation of anastomosis
Quantity: 17848 units
Why Was This Recalled?
Potential for the sterility barrier to be compromised.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LP
Covidien LP has 57 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report