IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol… — Class II medical device recall Z-1550-2013
Terminated recall by IDEV Technologies, Inc., reported 2013-06-26, distributed nationwide. There was an error on the outer labeling of this device. The inner label was correct.
| Recall number | Z-1550-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | IDEV Technologies, Inc., Webster, TX, United States |
| Recall initiated | 2012-05-29 |
| Classified | 2013-06-18 |
| Reported by FDA | 2013-06-26 |
| Terminated | 2013-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 3 |
| Reason classes | labeling |
| Lot numbers | 01049037 |
| Model numbers | S-05-100-120-G3 |
Product
IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms
Reason for recall
There was an error on the outer labeling of this device. The inner label was correct.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1550-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.