FDA Device recall Z-0371-2019
GE Healthcare Millennium MC
- FDA Device
- Class I
- terminated
- Published 2018-11-21
On 2018-11-21 the FDA classified a Class I recall of GE Healthcare Millennium MC by Ge Healthcare, citing A detector can detach and fall.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0371-2019 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2018-09-14 |
| Published | 2018-11-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV |
Product
GE Healthcare Millennium MC
Reason
A detector can detach and fall.
Identifiers
| code_info | System ID #: 870735MG, 928333WMM02, 970635MYO, 203576DNT, 407896FMG2, 954634MG, 316267KCN, 601883NMC2, 910483XEL1, 910…System ID #: 870735MG, 928333WMM02, 970635MYO, 203576DNT, 407896FMG2, 954634MG, 316267KCN, 601883NMC2, 910483XEL1, 910296MMG, 908277XL2, 908277MG2, 908218MYO, 918496EN1, 972759CROWNMG, 940566MG, 972434MC,and 972473MYO. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0371-2019%22
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