Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0495-2019)

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:

Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126

Product Classification:

Class II

Date Initiated: October 22, 2018

Date Posted: November 28, 2018

Recall Number: Z-0495-2019

Event ID: 81472

Reason for Recall:

Label on the outer carton or the patient labels does not match label on the inner sterile packaging

Status: Terminated

Product Quantity: 8 units

Code Information:

Lot Number: J6255863 UDI: (01)00880304270794(17)280411(10)J6265594

Distribution Pattern:

AR, MO, MN, NJ, NY, OH, MN , NJ, VA

Voluntary or Mandated:

Voluntary: Firm initiated