Reported Jun 26, 2013 · Terminated
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for…
IDEV Technologies, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: IDEV Technologies, Inc. · 253 Medical Center Blvd · Webster, TX · 77598-4213
Is this the product you have?
- IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms
- Lot codes and dates
- Model Number
S-05-100-120-G3Lot Number 01049037
- Model Number
- Amount recalled
- 3
Where it was sold
Why it was recalled
There was an error on the outer labeling of this device. The inner label was correct.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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