Magec 2 Rod recall
MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;
Why was Magec 2 Rod recalled?
Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.
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?
Version/Model: MC2-5090S; UDI-DI (with lot nuber): (01)00887517834041(11)250311(17)300311(10)GB1607ET
- Product
- MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;
- Recalling firm
- Globus Medical, Inc.
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution in the state of AR.
- Recall date
- April 30, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)