MAGEC 1 System recall
MAGEC 1 System
Why was MAGEC 1 System recalled?
Safety Alert to all surgeons informing them of post-implantation fractures of an internal metallic component for device manufactured prior to March 26, 2015.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 MAGEC Systems (Serial/Lot Numbers) manufactured prior to March 26, 2015.
- Product
- MAGEC 1 System
- Recalling firm
- NuVasive Specialized Orthopedics, Inc.
- Quantity
- 3,056 devices
- Distribution
- Worldwide
- Recall date
- February 2, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)