GE Healthcare, LLC Discovery NM670 Pro Model # H3100XB Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Discovery NM670 Pro Model # H3100XB
Brand
GE Healthcare, LLC
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Serial # PRGX52001 System ID: NMPRGX52001 Serial # PRGX52003 System ID: 082426210033 Serial # PRGX52008 System ID: 082426120037 Serial # PRGX52005 System ID: 082426120039 Serial # PRGX52007 System ID: 082426290010 Serial # PRGX52004 System ID: 082426180017 Serial # PRGX52009 System ID: 082426130053 Serial # PRGX52002 System ID:082426150044 Serial # PRGX52006 System ID:082426160065
GE Healthcare, LLC is recalling Discovery NM670 Pro Model # H3100XB due to Rotor bearing screws were found loose on detector.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Rotor bearing screws were found loose on detector.
Recommended Action
Per FDA guidance
GE Healthcare issued an Urgent Medical device correction notification on August 14, 2020. It states the following: 1. GE Healthcare will inspect and, if required, correct all affected products at no cost to you. 2. A GE Healthcare representative will contact you to arrange for the correction 3. Please complete the acknowledgement form and return it to GE Healthcare promptly upon receipt and no later than 30 days from receipt to nm.fmi40890.responses@ge.com If you have any questions or concerns regarding this notification, please contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, CT, FL, GA, IL, KS, KY, LA, MD, MA, MI, MN, MO, NE, NV, NJ, NY, OH, OK, RI, SC, TN, TX, VT, VA, WA, WI
Page updated: Jan 10, 2026