FDA Device recall Z-2994-2020
Discovery NM 630 Model # H3101RH
- FDA Device
- Class II
- terminated
- Published 2020-09-30
On 2020-09-30 the FDA classified a Class II recall of Discovery NM 630 Model # H3101RH by Ge Healthcare, citing rotor bearing screws were found loose on detector.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2994-2020 |
| 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
Discovery NM 630 Model # H3101RH
Reason
Rotor bearing screws were found loose on detector.
Identifiers
| code_info | Serial # 63GX50024 System ID: 501450D630 Serial # 63GX50001 System ID: 863494NM Serial # 63GX50037 System ID: 3v0522…Serial # 63GX50024 System ID: 501450D630 Serial # 63GX50001 System ID: 863494NM Serial # 63GX50037 System ID: 3v05223D630A Serial # 63GX50060 System ID: 305223D630B Serial # 63GX50017 Not Available Serial # 63GX50034 System ID: 478289DIS Serial # 63GX50040 System ID: 0004624609 Serial # 63GX50014 System ID: 618998NM Serial # 63GX50019 System ID: 270745NM1 Serial # 63GX50016 System ID: Not Available Serial # 63GX50022 System ID: 906225CARDNM1 Serial # 63GX50021 System ID: 906225CARDNM2 Serial # 63GX50018 System ID: 269637NM630 Serial # 63GX50009 System ID: NM555658 Serial # 63GX50031 System ID: Not Available Serial # 63GX50020 System ID: 402481D630C Serial # 63GX50054 System ID: 973450D630 Serial # 63GX50008 System ID: 856641NM Serial # 63GX50061 System ID: 702962NM1 Serial # 63GX50062 System ID: 702724NM1 Serial # 63GX50050 System ID: 702388DISC Serial # 63GX50043 Not Available Serial # 63GX50032 System ID: 513861NM Serial # 63GX50055 System ID: 513861NM1 Seria |
|---|
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-2994-2020%22
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