FDA Device recall Z-2001-2014
VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous ev…
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous ev… 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-2001-2014 |
| 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
VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 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 11786-37683 |
|---|
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-2001-2014%22
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