Discovery NM 630 Model # H3101RH — Class II medical device recall Z-2994-2020
Terminated recall by GE Healthcare, LLC, reported 2020-09-30, distributed in AR, CT, FL, GA, IL, KS, KY, LA…. Rotor bearing screws were found loose on detector.
| Recall number | Z-2994-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2020-08-14 |
| Classified | 2020-09-21 |
| Reported by FDA | 2020-09-30 |
| Terminated | 2021-05-06 |
| Distributed | 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 |
| Countries outside the US | AR, AT, BE, BR, CA, CH, CN, DE, ES, FR, GB, GR, IL, IN, IT, JP, KR, NL, NO, PA, PL, PT, RU, SE, TH, TR, TW, VN |
| Quantity | 62 units |
| Serial numbers | 63GX50001, 63GX50002, 63GX50003, 63GX50004, 63GX50005, 63GX50006, 63GX50007, 63GX50008, 63GX50009, 63GX50010, 63GX50011, 63GX50012, 63GX50013, 63GX50014, 63GX50015, 63GX50016, 63GX50017, 63GX50018, 63GX50019, 63GX50020, 63GX50021, 63GX50022, 63GX50023, 63GX50024, 63GX50025 and 37 more |
| Model numbers | H3101RH |
Product
Discovery NM 630 Model # H3101RH
Reason for recall
Rotor bearing screws were found loose on detector.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.