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FDA Medical Device Recalls (openFDA)

Zimmer, Inc.: NexGen Precoat Stemmed Tibial Plate Size 5

Recall number
Z-2092-2023
Recalling firm
Zimmer, Inc.
Product
NexGen Precoat Stemmed Tibial Plate Size 5
Status
Terminated
Initiated
2023-05-19
Posted
2023-07-05
Terminated
2026-05-29
Reason
Device outer packaging was incorrectly labeled.
Root cause
Under Investigation by firm
Action
The firm distributed recall notifications by email on 5/19/2023. Customers are asked to review the recall notification and distribute to team members so they are aware of its contents. Additionally, customers are to identify and quarantine any affected devices, complete the provided Inventory Return Certification form, and ship affected product back to Zimmer. Customers are to retain a copy of the Inventory Return Certification for their records. Customers with any questions may call 574-371-3071 or email CorporateQuality.PostMarket@zimmerbiomet.com.
Quantity
not on file
Distribution
International distribution in the country of India.
Lot, serial or model codes
Model No. 00598004701; UDI No./Lot. No.: (01)00889024217607(17)321228(10)J7418537/J7418537 and (01)00889024217607(17)321228(10)J7418542/J7418542.
510(k) numbers
["K173057"]
PMA numbers
not on file
Product code
JWH
Firm FEI
1000220733
Firm city
Warsaw
Firm state
IN
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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