07-150-07 MIZUHO — Class II medical device recall Z-1998-2014
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-1998-2014 |
|---|---|
| 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 | 164 |
| Reason classes | sterility |
| Lot numbers | 11798-37631 |
| Model numbers | 138200 |
Product
07-150-07 MIZUHO, MAL DISP DOPPLER PROBE BX 4, REF 138200 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-1998-2014. 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.