Summary
The FDA issued a Class II for Snapshot NIR, REF: KD204 by KENT IMAGING, INC.. Reason: Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images..
Details
Source
Device Recall
External ID
Z-0789-2024
Action Date
2024-01-31
Status
Ongoing
Category
device
Product Description
Snapshot NIR, REF: KD204
Lot/Code Info: UDI-DI: B376KD2040, Serial Numbers: 204TUC1001, 204TUC1002, 204TUC1003, 204TUC1004, 7204TUC1005, 204TUC1006, 204TUC1007, 204TUC1008, 204TUC1009, 204TUC1010, 204TUC1011, 204TUC1012, 204TUC1013, 204TUC1014, 204TUC1015, 204TUC1024, 204TUC1025, 204TUC1026, 204TUC1028, 204TUC1029, 204TUC1033, 204TUC1036, 204TUC1038, 204TUC1040, 204TUC1041, 204TUC1042, 204TUC1043
Quantity Affected: 57
Reason for Recall
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-30
Company
Calgary, N/A
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 144 device recalls issued in the same week, part of 403 device-related FDA actions this month.
KENT IMAGING, INC. has 3 FDA actions in our database, including 1 recall and 2 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KENT IMAGING, INC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KENT IMAGING, INC. have FDA actions?
KENT IMAGING, INC. has 3 FDA actions in our database, including 1 recall and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0789-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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