GE Healthcare, LLC: Medical Device Recall in 2020 - (Recall #: Z-2997-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Discovery NM670 Pro Model # H3100XB

Product Classification:

Class II

Date Initiated: August 14, 2020

Date Posted: September 30, 2020

Recall Number: Z-2997-2020

Event ID: 86337

Reason for Recall:

Rotor bearing screws were found loose on detector.

Status: Terminated

Product Quantity: 9 units

Code Information:

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

Distribution Pattern:

USA : 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 OUS: ARGENTINA AUSTRIA BELGIUM BRAZIL Canada CHINA FRANCE GERMANY GREECE INDIA ISRAEL ITALY JAPAN Korea (Republic of) NETHERLANDS NORWAY PANAMA POLAND PORTUGAL Russia SPAIN SWEDEN SWITZERLAND TAIWAN THAILAND TURKEY UNITED KINGDOM VIETNAM

Voluntary or Mandated:

Voluntary: Firm initiated