Kent Imaging, Inc. FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.Class IIJun 30, 2026The software controlling the wound imaging device's battery	The software controlling the wound imaging device's battery charging circuit was not designed to recognize and	Class IIDevices	Jun 30, 2026
Snapshot NIR, REF: KD204Class IIOct 30, 2023Tissue oxygenation measurement system touchscreens may be un	Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxyge	Class IIDevices	Oct 30, 2023