The UNI-CP System recall
The UNI-CP System; Model Number: 330230SND.
Why was The UNI-CP System recalled?
The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.
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 # FEDT
- Product
- The UNI-CP System; Model Number: 330230SND.
- Recalling firm
- Integra LifeSciences Corp.
- Quantity
- 39 units
- Distribution
- Nationwide
- Recall date
- March 15, 2017
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)