KENT IMAGING, INC.: Medical Device Recall in 2024 - (Recall #: Z-0789-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Snapshot NIR, REF: KD204

Product Classification:

Class II

Date Initiated: October 30, 2023

Date Posted: January 31, 2024

Recall Number: Z-0789-2024

Event ID: 93624

Reason for Recall:

Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.

Status: Ongoing

Product Quantity: 57

Code Information:

UDI-DI: B376KD2040, Serial Numbers: 204TUC1001, 204TUC1002, 204TUC1003, 204TUC1004, 7204TUC1005, 204TUC1006, 204TUC1007, 204TUC1008, 204TUC1009, 204TUC1010, 204TUC1011, 204TUC1012, 204TUC1013, 204TUC1014, 204TUC1015, 204TUC1024, 204TUC1025, 204TUC1026, 204TUC1028, 204TUC1029, 204TUC1033, 204TUC1036, 204TUC1038, 204TUC1040, 204TUC1041, 204TUC1042, 204TUC1043

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of IN, OH, TX, PA, WI, OR, CO, IL, MO, CA, AZ, IA and the countries of Malaysia.

Voluntary or Mandated:

Voluntary: Firm initiated