Zimmer, Inc.: Medical Device Recall in 2012 - (Recall #: Z-1980-2012)

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 3573-1 (angle handle) , Stainless Steel / Silicone Rubber, Rx only, non sterile. Product Usage: The rod is held by the instrument for inserting and guiding into the screw heads via percutaneous delivery during minimally invasive surgery to fuse the spine. Per the surgical technique (Ll554 Pathfinder NXT Surgical Technique);

Product Classification:

Class II

Date Initiated: June 5, 2012

Date Posted: July 18, 2012

Recall Number: Z-1980-2012

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 3573-1 (angle handle) all lots including 64PY, 67YA, 69FF, 71GB, 72JL, 73GY

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