Class II — Potential Health Hazard

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

MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582 Recalled by Siemens Medical Solutions USA, Inc Due to Potential of an open port in the quench...

Date: July 9, 2019
Company: Siemens Medical Solutions USA, Inc
Status: Terminated
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

MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582

Quantity: 17

Why Was This Recalled?

Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.

Where Was This Sold?

This product was distributed to 41 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MO, MT, NE, NH, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, VA, WA, WV, WI, WY, DC

Affected (41 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