NexGen Precoat Stemmed Tibial Plate recall
NexGen Precoat Stemmed Tibial Plate Size 5
Why was NexGen Precoat Stemmed Tibial Plate recalled?
Device outer packaging was incorrectly labeled.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model No. 00598004701; UDI No./Lot. No.: (01)00889024217607(17)321228(10)J7418537/J7418537 and (01)00889024217607(17)321228(10)J7418542/J7418542.
- Product
- NexGen Precoat Stemmed Tibial Plate Size 5
- Recalling firm
- Zimmer, Inc.
- Quantity
- N/A
- Distribution
- International distribution in the country of India.
- Recall date
- July 12, 2023
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)