Nextra Hammertoe Correction System Driver recall
Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument
Why was Nextra Hammertoe Correction System Driver recalled?
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
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?
Lot Number: 168A27917C UDI: 00817701020837
- Product
- Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument
- Recalling firm
- Nextremity Solutions
- Quantity
- 239 units
- Distribution
- Distribution US Nationwide, Japan, and the Netherlands
- Recall date
- April 20, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)