Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0938-2019)

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:

Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766

Product Classification:

Class II

Date Initiated: December 21, 2018

Date Posted: March 6, 2019

Recall Number: Z-0938-2019

Event ID: 82004

Reason for Recall:

Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.

Status: Terminated

Product Quantity: 90 units

Code Information:

Lot Number: 381800 UDI Number: (01)00880304434349(17)230301(10)381800 Lot NUmber: 400030 (01)00880304434349(17)230329(10)400030

Distribution Pattern:

MN, VA Foreign: Korea, New Zealand and Japan

Voluntary or Mandated:

Voluntary: Firm initiated