IDEV Technologies SUPERA VERITAS Interwoven recall: Labeling Error
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary…
Why was IDEV Technologies SUPERA VERITAS Interwoven recalled?
There was an error on the outer labeling of this device. The inner label was correct.
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?
Model Number: S-05-100-120-G3; Lot Number 01049037
- Product
- IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary…
- Recalling firm
- IDEV Technologies, Inc.
- Quantity
- 3
- Distribution
- Nationwide Distribution to the states of FL, NY, and PA.
- Recall date
- June 26, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)