Product Safety Recalls

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Zimmer, Inc. Recall 92531

Description: NexGen Precoat Stemmed Tibial Plate Size 5

Zimmer, Inc. Recall 92531 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-2092-2023
Event ID92531
Event DescriptionNexGen Precoat Stemmed Tibial Plate Size 5
Product TypeDevices
DistributionInternational distribution in the country of India.
Recall ReasonDevice outer packaging was incorrectly labeled.
Device Classification20230712
Device Code InfoModel No. 00598004701; UDI No./Lot. No.: (01)00889024217607(17)321228(10)J7418537/J7418537 and (01)00889024217607(17)321228(10)J7418542/J7418542.
Center Classification Date20230705
Recall Initiation Date20230519
Recalling FirmZimmer, Inc.
Initial Notification Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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