FDA Device recall Z-2344-2019
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
- FDA Device
- Class II
- terminated
- Published 2019-08-28
On 2019-08-28 the FDA classified a Class II recall of MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643 by Siemens Medical Solutions Usa, citing potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2344-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-09 |
| Published | 2019-08-28 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, 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 |
Product
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Reason
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Identifiers
| code_info | Serial # 72030 72023 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2344-2019%22
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