SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
KENT IMAGING, INC.
The hazard
The software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully discharged into a low-power "shipping mode." When this occurs, an affected device will not resume charging when reconnected to power and becomes temporarily unusable/ unavailable for wound imaging until corrected. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI-DI: B376KB1000Model Software Revisions v4.2.0 and v4.1.3Would you have heard about this one?
RapidRecall watches everything you own against every new federal recall and emails you the moment something you bought turns up. Free for your most important items.
Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.