Biomet, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0364-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless Soft Anchors are indicated for soft tissue reattachment procedures in the shoulder, foot/ankle, hand/wrist, and hip.

Product Classification:

Class II

Date Initiated: October 10, 2013

Date Posted: November 27, 2013

Recall Number: Z-0364-2014

Event ID: 66639

Reason for Recall:

Investigation identified that the design of the drill bit may make the suture anchor difficult to insert into the bone. The implant may skip across the hole or miss the hole during insertion.

Status: Terminated

Product Quantity: 25

Code Information:

Catalog:110003173, Lot 127480, 185420, 233500, 233520

Distribution Pattern:

USA Nationwide Distribution in the states of VA, CA, Ky, and IN

Voluntary or Mandated:

Voluntary: Firm initiated