FDA Device recall Z-2993-2020
NM/CT 870 CZT Model # H3906CW
- FDA Device
- Class II
- terminated
- Published 2020-09-30
On 2020-09-30 the FDA classified a Class II recall of NM/CT 870 CZT Model # H3906CW by Ge Healthcare, citing rotor bearing screws were found loose on detector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2993-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-08-14 |
| Published | 2020-09-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | AR, CT, FL, GA, IL, KS, KY, LA, MA, MD, MI, MN, MO, NE, NJ, NV, NY, OH, OK, RI, SC, TN, TX, VA, VT, WA, WI |
Product
NM/CT 870 CZT Model # H3906CW
Reason
Rotor bearing screws were found loose on detector.
Identifiers
| code_info | Serial # 87CX63007 System ID: AH0101NM05 Serial # 87CX63008 System ID: 190020NU01 Serial # 87CX63006 System ID: 03024…Serial # 87CX63007 System ID: AH0101NM05 Serial # 87CX63008 System ID: 190020NU01 Serial # 87CX63006 System ID: 030240NU11 Serial # 87CX63015 System ID: 705743NM870 Serial # 87CX63014 System ID: 030078NU28 Serial # 87CX63011 System ID: M4184879 Serial # 87CX63003 System ID: M9886873 Serial # 87CX63004 System ID: X171582003 Serial # 87CX63009 System ID: M171582018 Serial # 87CX63010 System ID: UC1796NU01 Serial # 87CX63013 System ID: NO1068MN18 Serial # 87CX63005 System ID: A004NU20 Serial # 87CX63002 System ID: C028NU01 Serial # 87CX63012 System ID: C028NU02 Serial # 87CX63001 System ID: 900010NU12 |
|---|
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-2993-2020%22
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