FDA Device recall Z-1999-2014
07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation…
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of 07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation… by Vascular Technology, citing report of the product penetrating the sterile barrier; this could render the product unsterile.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1999-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-28 |
| Published | 2014-07-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Vascular Technology |
| Distribution | CA |
Product
07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
Reason
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Identifiers
| code_info | LOT NUMBER 11802-37667 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1999-2014%22
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