07-150-12 MIZUHO — Class II medical device recall Z-2000-2014
Terminated recall by Vascular Technology, Inc., reported 2014-07-16, distributed in CA. Report of the product penetrating the sterile barrier; this could render the product unsterile.
| Recall number | Z-2000-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vascular Technology, Inc., Nashua, NH, United States |
| Recall initiated | 2014-05-28 |
| Classified | 2014-07-07 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2016-02-11 |
| Distributed | CA |
| Countries outside the US | AU, GB, TW |
| Quantity | 34 |
| Reason classes | sterility |
| Lot numbers | 1516-37698 |
| Model numbers | 138665 |
Product
07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
Reason for recall
Report of the product penetrating the sterile barrier; this could render the product unsterile.
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-2000-2014. 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.