Calgary, N/A, Canada
KENT IMAGING, INC. recalls
2 recalls recorded since 2018, most recently on 30 June 2026. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 30 June 2026
- Reason
- 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.
- Distribution
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT, IN, DC, KS, IL, TN, AR, AZ.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2775-2026
- SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Ongoing Class II Medical devices
- Recall started
- 30 October 2023
- Reason
- Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.
- Distribution
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0789-2024
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.