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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: INSET¿; INSET I 60/6 GREY
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INSET¿; INSET I 60/6 GREY Back to Search Results
Lot Number 5163025
Medical Device Problem Code Material Twisted/Bent (2981)
Health Effect - Clinical Code Elevated ketones/Diabetic Ketoacidosis (2364)
Type of Reportable Event Serious Injury
Event or Problem Description
Unomedical reference number: (b)(4).Event occurred in united states.The patient reported that her infusion set's cannula was kinked.Reportedly, her blood glucose was more than 600 mg/dl and she experienced diabetic ketoacidosis.She self-treated with a correction bolus.Subsequently, she was admitted in the hospital, where she received some unspecified fluids and insulin drip as corrective treatment which resolved the issue.She was hospitalized for four days and there was no permanent damage to the patient.The infusion set was used for less than three days.Reportedly, her blood glucose had come back to the target.Unomedical do not see bent/kinking as being related to human factors, but rather as a training issue including correct choices of insertion sites and infusion sets and cannula length.Furthermore, the soft cannula is a flexible material that during use and upon removal can bend slightly.No further information available.
 
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Brand Name
INSET¿
Common Device Name
INSET I 60/6 GREY
MDR Report Key8538554
Report Number3003442380-2019-01343
Device Sequence Number2443686
Product Code FPA
UDI-Device Identifier05705244006874
UDI-Public05705244006874
Combination Product (Y/N)N
PMA/510(K) Number
K032854
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source distributor
Initial Reporter Occupation Other
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device No Information
Device Lot Number5163025
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 03/15/2017
Initial Report FDA Received Date04/23/2019
Patient Sequence Number1
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