# FDA recall Z-2345-2019

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-07-09.

## Product

MAGNETOM Prisma magnetic resonance diagnostic devices   Model #10849582

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-2345-2019
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-09
- **Report date:** 2019-08-28
- **Termination date:** 2020-04-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2345-2019

## Citation

> AI Analytics. FDA recall Z-2345-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2345-2019. Source: US FDA. Licensed CC0.

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