Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a separation and an insufficient...
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 Biomet, Inc. directly.
Affected Products
Green Mamba Suture Passer
Quantity: 13
Why Was This Recalled?
There may be a separation and an insufficient weld between the spring and washer. The weld between the spring and washer may fracture, causing the Mamba Suture Passer instruments jaw to not actuate properly. 6 complaints have been received in which 3 have been reported with a delay up to 10 minutes.
Where Was This Sold?
This product was distributed to 20 states: AL, AR, CA, FL, GA, HI, IN, KS, KY, LA, MN, MO, NJ, NY, NC, OH, TX, UT, VA, WI
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report