Zimmer, Inc.: Medical Device Recall in 2012 - (Recall #: Z-1981-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-2 (straight handle) Stainless Steel / Silicone Rubber, Rx only, non sterile. Product Usage: PathFinder NXT is a minimally invasive pedicle screw system. The PathFinder NXT System consists of various screws and rods intended to provide temporary stabilization following surgery to fuse the spine. The intended use of the Fixed Angled Percutaneous Rod Inserter is to insert a rod percutaneously through the extender sieeves to position into the implanted screw heads for securing with closure tops forming a construct that provides temporary stabilization following MIS or mini-open surgery to fuse the spine.

Product Classification:

Class II

Date Initiated: June 5, 2012

Date Posted: July 18, 2012

Recall Number: Z-1981-2012

Event ID: 62325

Reason for Recall:

Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because complaints have been received that the rod holder tip may crack or break when the rod is manipulated during surgery.

Status: Terminated

Product Quantity: 249 ( angle handle and straight) in total

Code Information:

Part numbers 3573-2 (straight handle) all lots.

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and the countries of: Austria, Australia, Belgium, France, Gelmany, Italy, Spain, Switzerland and the United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated