RecallRadar

FDA Device recall Z-2998-2020

NM/CT 870 DR Model # H3100AS

On 2020-09-30 the FDA classified a Class II recall of NM/CT 870 DR Model # H3100AS by Ge Healthcare, citing rotor bearing screws were found loose on detector.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2998-2020
ClassificationClass II
Statusterminated
Initiated2020-08-14
Published2020-09-30
Last updated2026-09-13 11:55 UTC
CompanyGe Healthcare
DistributionAR, 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 DR Model # H3100AS

Reason

Rotor bearing screws were found loose on detector.

Identifiers

code_info
Serial # 870X64001 System ID: 030020NU06 Serial # 870X64004 System ID: M4018555 Serial # 870X64012 System…Serial # 870X64001 System ID: 030020NU06 Serial # 870X64004 System ID: M4018555 Serial # 870X64012 System ID: X634445001 Serial # 870X64007 System ID: V2728113 Serial # 870X64009 System ID: M4016255 Serial # 870X64026 System ID: M40230109 Serial # 870X64017 System ID: M40240121 Serial # 870X64018 System ID:M40240121 Serial # 870X64015 System ID:M40345223 Serial # 870X64016 System ID:499221NU01 Serial # 870X64031 System ID:083049209623319 Serial # 870X64014 System ID:IL1028NM41 Serial # 870X64022 System ID: A5173220 Serial # 870X64019 System ID: 0850260167XE6 Serial # 870X64020 System ID: 0850260169 Serial # 870X64025 System ID: EMM0135 Serial # 870X64010 System ID:NM2882PA Serial # 870X64027 System ID: PL0398NM01 Serial # 870X64029 System ID: PL1031NM01 Serial # 870X64030

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-2998-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.