SnapshotGLO Wound Imaging Device — Class II medical device recall Z-2775-2026
Ongoing recall by KENT IMAGING, INC., reported 2026-07-29, distributed nationwide. The software controlling the wound imaging device's battery charging circuit was not designed to recognize and
| Recall number | Z-2775-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | KENT IMAGING, INC., Calgary, N/A, Canada |
| Recall initiated | 2026-06-30 |
| Classified | 2026-07-22 |
| Reported by FDA | 2026-07-29 |
| Distributed | Nationwide (US) |
| Quantity | 77 |
| Reason classes | software |
| Model numbers | KB100, KB100AA |
Product
SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2775-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.