PlainRecalls
FDA Devices Moderate Class II Terminated

Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764

Reported: March 6, 2019 Initiated: December 21, 2018 #Z-0937-2019

Product Description

Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764

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.

Details

Recalling Firm
Zimmer Biomet, Inc.
Units Affected
45 units
Distribution
MN, VA Foreign: Korea, New Zealand and Japan
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Vanguard Knee System Series-A Standard Patella sizes 31mm Item Number: 184764. Recalled by Zimmer Biomet, Inc.. Units affected: 45 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 6, 2019. Severity: Moderate. Recall number: Z-0937-2019.