FDA Device recall Z-0199-2019
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces cross-sectional transa…
- FDA Device
- Class II
- ongoing
- Published 2018-10-31
On 2018-10-31 the FDA classified a Class II recall of Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces cross-sectional transa… by Canon Medical System Usa, citing when using respiratory gating with Steady Mode ON in Spin Echo sequence scanning, the SAR (Specific Absorption Rate) value displayed on the console may be lower than the actual SA….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0199-2019 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-05-30 |
| Published | 2018-10-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Canon Medical System Usa |
| Distribution | AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, MS, MT, NC, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VT, WA, WI, WV, WY |
Product
Nuclear Magnetic Resonance Imaging Systems that are indicated for use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or body.
Reason
When using respiratory gating with Steady Mode ON in Spin Echo sequence scanning, the SAR (Specific Absorption Rate) value displayed on the console may be lower than the actual SAR value. The actual applied SAR values may exceed the FIRST LEVEL CONTROLLED OPERATING MODE.
Identifiers
| code_info | MODEL SERIAL NUMBER SID MEXL-1504/U4 U4A12Z2020 30005914 MEXL-1504/T4 S4D1132069 339325 MEXL-1504/…MODEL SERIAL NUMBER SID MEXL-1504/U4 U4A12Z2020 30005914 MEXL-1504/T4 S4D1132069 339325 MEXL-1504/S4 S4A1032017 326165 MEXL-1504/U4 U4A1312023 30000547 MEXL-1504/S4 S4A1032019 327601 MEXL-1504/U4 U4A1312024 30002325 MEXL-1504/T4 S4D1152082 330035 MEXL-1504/S4 S4A1082040 330134 MEXL-1504/A4 A4A11Z2011 346866 MEXL-1504/U4 U4A1282003 356105 MEXL-1504/U4 U4A1322025 30009003 MEXL-1504/U4 U4B1442070 30012516 MEXL-1504/U4 U4A1352035 389636 MEXL-1504/U4 U4B1552097 30010318 MEXL-1504/U4 U4A12X2010 351817 MEXL-1504/S4 S4C1112065 330381 MEXL-1504/S4 S4C1112064 334599 MEXL-1504/A4 A4A11Z2009 352039 MEXL-1504/S4.004 S4A1072033 30025756 MEXL-1504/S4 S4A09Y2002 345231 MEXL-1504/U4.004 U4A1282002 30027784 MEXL-1504/U4.004 U4A1382047 30036224 MEXL-1504/S3 S3A0972030 312421 MEXL-1504/U4 U4A12X2011 345074 MEXL-1504/S4 S4C1112061 337212 MEXL-1504/U4 U4A13X2054 30011038 MEXL-1504/A4 A4A1222015 351023 MEXL-1504/U4 U4A1322026 337071 MEXL-1504/U4 U4B1642106 30008 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0199-2019%22
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