Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0338-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

cable button for NCB¿ Polyaxial Locking Plate, 2.5 mm Hex Drive, Item No. 47223206001

Product Classification:

Class II

Date Initiated: October 10, 2019

Date Posted: November 13, 2019

Recall Number: Z-0338-2020

Event ID: 83962

Reason for Recall:

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Status: Terminated

Product Quantity: 5459583 total devices

Code Information:

12752657 12784266 12784266 12784266 12778187 12778187 12752661 12784267 12784267 12784267 12776194 12784268 12784268 12784268 12774326 12753709 12753702 12753707 12784261

Distribution Pattern:

Distributed nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated