Reusable instruments in the Knee recall
Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
Why was Reusable instruments in the Knee recalled?
Durability characteristics of reusable instruments were not established
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?
All lots in distribution prior to 5/8/17
- Product
- Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- Greater than 10,000,000 last 10 years
- Distribution
- Nationwide Worldwide
- Recall date
- June 7, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)