KENT IMAGING, INC. recalls
Every recall we track for KENT IMAGING, INC. — 2 in all, from 2023–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for KENT IMAGING, INC. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled KENT IMAGING, INC. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All KENT IMAGING, INC. recalls
2 shown- Lower riskMedical device
KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
KENT IMAGING recalls SnapshotGLO Wound Imaging Device models KB100 and KB100AA due to battery charging software issues that cause temporary unavailability after full discharge.
KENT IMAGINGJun 30, 2026 - Lower riskMedical device
KENT IMAGING, INC. recalls Snapshot NIR, REF: KD204
Kent Imaging recalls Snapshot NIR REF KD204 devices with unresponsive touchscreens that may prevent viewing oxygenation images. Affected units have specific serial numbers and UDI-DI codes.
Kent ImagingOct 30, 2023
KENT IMAGING, INC. recall questions
How many recalls has KENT IMAGING, INC. had?
2 recalls from KENT IMAGING, INC. are on record with U.S. safety agencies, from 2023–2026.
What is the most recent KENT IMAGING, INC. recall?
KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device, Model KB100, KB100AA., dated Jun 30, 2026. Every KENT IMAGING, INC. recall is listed on this page, newest first.
What should I do if I have a recalled KENT IMAGING, INC. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new KENT IMAGING, INC. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.