Zimmer, Inc.: Medical Device Recall in 2023 - (Recall #: Z-2092-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

NexGen Precoat Stemmed Tibial Plate Size 5

Product Classification:

Class II

Date Initiated: May 19, 2023

Date Posted: July 12, 2023

Recall Number: Z-2092-2023

Event ID: 92531

Reason for Recall:

Device outer packaging was incorrectly labeled.

Status: Ongoing

Product Quantity: N/A

Code Information:

Model No. 00598004701; UDI No./Lot. No.: (01)00889024217607(17)321228(10)J7418537/J7418537 and (01)00889024217607(17)321228(10)J7418542/J7418542.

Distribution Pattern:

International distribution in the country of India.

Voluntary or Mandated:

Voluntary: Firm initiated