Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1522-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar, Model Number CP260600 Product Usage: The replacement of segmental defects of long bone, including midshaft replacement, and arthrodesis of the knee.

Product Classification:

Class II

Date Initiated: April 3, 2018

Date Posted: May 2, 2018

Recall Number: Z-1522-2018

Event ID: 79692

Reason for Recall:

There is a potential dry blast irregularity on the locking collar screws packaged with the locking collar.

Status: Terminated

Product Quantity: 16 units (21 distribution events. The product is lot controlled and may be distributed multiple times if it was returned and returned to the shelf)

Code Information:

Lot Number 360610, 333020

Distribution Pattern:

The product was distributed to the following states: CT, FL, GA, IN, MA, MI, NY, and TX. The product was distributed to the following countries: Malaysia and Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated