Zimmer Manufacturing B.V.: Medical Device Recall in 2016 - (Recall #: Z-1341-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in total knee arthroplasty. REF 42-5114-008-18

Product Classification:

Class II

Date Initiated: March 17, 2016

Date Posted: April 13, 2016

Recall Number: Z-1341-2016

Event ID: 73498

Reason for Recall:

The firm received a customer complaint establishing that the product (Persona PS Articular Surfaces)information shown on the box differed by sides. One side showed P/N: 42-5114-008-18/ Lot: 62632101 and the other side showed P/N: 42-5114-005-14/ Lot: 62646580.

Status: Terminated

Product Quantity: TBD

Code Information:

lot 62632101

Distribution Pattern:

Distributed in US (AL, AZ, CA, GA, HI, ID, KS, LA, MA, MN, MO, NY, OH, OK, PA, TX, UT, VA, and WI) and foreign countries (Korea, Japan, Germany, Singapore, Austria, Italy, South Africa, and Spain).

Voluntary or Mandated:

Voluntary: Firm initiated