Biomet, Inc.: Medical Device Recall in 2015 - (Recall #: Z-0472-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Green Mamba Suture Passer

Product Classification:

Class II

Date Initiated: December 2, 2015

Date Posted: December 30, 2015

Recall Number: Z-0472-2016

Event ID: 72829

Reason for Recall:

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.

Status: Terminated

Product Quantity: 13

Code Information:

Catalog Number: 110010850 Lot Number Identification: 167890, 231120, 253210, 550050, 551580, 716300, 953230

Distribution Pattern:

FL, NJ, WI, UT, TX, KY, KS, OH, GA, LA, AL, NY, NC, AR, MO, VA, CA, MN, IN, HI

Voluntary or Mandated:

Voluntary: Firm initiated