Starburst MRI Semi-Flex Electrode Device — Class II medical device recall Z-1143-2015
Terminated recall by Angiodynamics, reported 2015-03-04, distributed in AR, AZ, FL, MI, MN, MO, NY, TX…. Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually l
| Recall number | Z-1143-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Angiodynamics, Glens Falls, NY, United States |
| Recall initiated | 2014-12-19 |
| Classified | 2015-02-24 |
| Reported by FDA | 2015-03-04 |
| Terminated | 2015-11-27 |
| Distributed | AR, AZ, FL, MI, MN, MO, NY, TX, VA, WA, WI |
| Countries outside the US | ES, HU |
| Quantity | 43 |
| Lot numbers | 4773676, 4776428, 4780110 |
| Model numbers | 700-102615, 700-103909 |
Product
Starburst MRI Semi-Flex Electrode Device, 25cm/Attached Cable/14Ga/6.4F, Product No. H7877001039091, Catalog No. 700-103909; 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615; and 25cm/14Ga/6.4F, Product No. H7877001026151, Catalog No. 700-102615
Reason for recall
Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually located 4cm from the distal tip of the needle.
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-1143-2015. 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.