FDA Device recall Z-2000-2014
07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluat…
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of 07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluat… 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-2000-2014 |
| 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
07-150-12 MIZUHO, MINI, SLIM, STERILE, BOX OF 4, REF 138665 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.
Reason
Report of the product penetrating the sterile barrier; this could render the product unsterile.
Identifiers
| code_info | LOT NUMBER 1516-37698 |
|---|
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-2000-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.