Reported Jan 31, 2024 · Ongoing
Snapshot NIR, REF: KD204
Kent Imaging, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: KENT IMAGING, INC. · Suite 300, 1210 8 Street SW · Calgary, N/A · N/A
Is this the product you have?
- Snapshot NIR
- REFKD204
- Lot codes and dates
- UDI-DIB376KD2040
- Serial Numbers
204TUC1001204TUC1002204TUC1003204TUC10047204TUC1005204TUC1006204TUC1007204TUC1008204TUC1009204TUC1010204TUC1011204TUC1012204TUC1013204TUC1014204TUC1015204TUC1024204TUC1025204TUC1026204TUC1028204TUC1029204TUC1033204TUC1036204TUC1038204TUC1040204TUC1041204TUC1042204TUC1043
- Amount recalled
- 57
Where it was sold
Why it was recalled
Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Kent Imaging, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.