PlainRecalls
FDA Devices Moderate Class II Ongoing

NexGen Precoat Stemmed Tibial Plate Size 5

Reported: July 12, 2023 Initiated: May 19, 2023 #Z-2092-2023

Product Description

NexGen Precoat Stemmed Tibial Plate Size 5

Reason for Recall

Device outer packaging was incorrectly labeled.

Details

Recalling Firm
Zimmer, Inc.
Units Affected
N/A
Distribution
International distribution in the country of India.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
NexGen Precoat Stemmed Tibial Plate Size 5. Recalled by Zimmer, Inc.. Units affected: N/A.
Why was this product recalled?
Device outer packaging was incorrectly labeled.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 12, 2023. Severity: Moderate. Recall number: Z-2092-2023.