KENT IMAGING, INC. recalls SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
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…
Read the official notice →- Date
- 2026-07-29
- Country
- United States
- Brand
- Kent Imaging
- Product
- SnapshotGLO Wound Imaging Device, Model KB100, KB100AA.
- Classification
- Class II
- Units
- US Nationwide distribution in the states of PA, IA, FL, TX, GA, NV, CA, UT,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Kent Imaging recalls
- 2024-01-31
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Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.
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Other drugs & medical recalls in the United States
- 2026-07-29
- US
Medtronic MiniMed, Inc. recalls MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated alerts will not be triggered during the nighttime. This…
FDA · DeviceMedtronic MiniMed, Inc.Worldwide - US Nationwide distribution in the states and territories of PR,…Official notice → - US
Emano Metrics, Inc. recalls Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is a smartphone-based acoustic uroflowmetry system.…
Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model was trained and validated on 44,100 Hz audio. The models…
FDA · DeviceEmano Metrics, Inc.U.S. Nationwide distribution in the states of AR, AZ, CA, CO, FL. IA, ID, NC,…Official notice → - US
Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit - UHI-4. Model Number: UHI-4
Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases.
FDA · DeviceOlympus Corporation of the AmericasWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
Micro Therapeutics, Inc. recalls Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 REF PED2-300-20. Intracranial aneurysm flow diverter
Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20 mm implants.
FDA · DeviceMicro Therapeutics, Inc.US Nationwide distribution in the states of CT, DE, IN, MA, NC, NJ, NM, NY,…Official notice → - US
AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.
FDA · DeviceAVID Medical, Inc.U.S. Nationwide distribution in the state of California.Official notice → - US
Boston Scientific Corporation recalls Boston Scientific TheraSphere 360 Y-90 Management Platform, Model Number M00139509001; Radiological Image Processing System.
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a user modifies an input and selects "Recalculate", the dose…
FDA · DeviceBoston Scientific CorporationUS Nationwide distribution including in the states of AL, AR, AZ, CA, CO, FL,…Official notice →