Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Sensis Vibe Hemo Recalled by Siemens Medical Solutions USA, Inc Due to The possibility of the Sensis documentation functionality application...

Date: November 29, 2023
Company: Siemens Medical Solutions USA, Inc
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.

Affected Products

Sensis Vibe Hemo

Quantity: 331 units

Why Was This Recalled?

The possibility of the Sensis documentation functionality application to crash.

Where Was This Sold?

This product was distributed to 3 states: CA, CT, FL

Affected (3 states)Not affected

About Siemens Medical Solutions USA, Inc

Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report