GE Healthcare, LLC: Medical Device Recall in 2019 - (Recall #: Z-1964-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D

Product Classification:

Class II

Date Initiated: July 2, 2019

Date Posted: July 24, 2019

Recall Number: Z-1964-2019

Event ID: 83271

Reason for Recall:

Potential for a transducer mis-alignment in certain transvaginal probes.

Status: Terminated

Product Quantity: 3 devices

Code Information:

Model KTZ303987-R - Serial Number (UDI Number): 226914KR0 (01008406821084301118032721226914KR0), 198026KR7 (Not Available), 220616KR7 (01008406821084301117091521220616KR7), 205375KR9 (01008406821085531116071121205375KR9)

Distribution Pattern:

Distribution in the US to Texas. International distribution to France, Greece and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated