FDA Recall Terminated

Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba instruments are utilized to aid in passing suture through soft tissue. The Mamba Needle is designed for use with the Mamba Suture Passer. The needles are sterile, disposable, and for single-patient use only.

Recall: Z-0058-2015 · Initiated September 26, 2014

Recall

Recall Number
Z-0058-2015
Event Number
69360
Firm
Biomet, Inc.
FEI Number
1825034
Product Code
HXQ
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
September 26, 2014
Posted
October 9, 2014
Terminated
July 14, 2015
Address
56 E Bell Dr, Warsaw, IN, 46581

Description

Mamba Disposable Nitinol Needle. The Biomet Sports Medicine Mamba instruments are utilized to aid in passing suture through soft tissue. The Mamba Needle is designed for use with the Mamba Suture Passer. The needles are sterile, disposable, and for single-patient use only.

Reason

An investigation identified that high level friction may exist between the needle and Mamba suture passer instrument, causing the needle to break during use.

Action

On 9/26/2014, "URGENT MEDICAL DEVICE RECALL NOTICE" notifications were sent via courier to the affected distributors with instructions for returning the affected product. The recall notification included a description of the reason for the recall, affected product, consignee responsibilities, contact information, and instructions for responding to the formal recall notification.

Distribution

Nationwide Distribution-including the states of FL, NY, TX, VA, NV, MI, CA, IN, SD, GA, KY, NC, and AR.

Quantity

164 units