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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AUTOSOFT XC UNO INSET I 60/9 GREY TCAP 10PK INT

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AUTOSOFT XC UNO INSET I 60/9 GREY TCAP 10PK INT Back to Search Results
Model Number 1001681
Device Problem Detachment of Device or Device Component (2907)
Patient Problem Hyperglycemia (1905)
Event Type  malfunction  
Event Description
Unomedical reference number (b)(4). Event occurred in the united states. It was reported that on (b)(6) 2022, the patient's infusion set's tubing detached/broken at the site connector. Therefore, her blood glucose level was high at the time of the event which they tried to treat with correction bolus via multiple daily injection. The infusion set had been used for the first day. Moreover, they replaced the infusion set and insulin was resumed successfully. No further information available.
 
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Brand NameAUTOSOFT XC
Type of DeviceUNO INSET I 60/9 GREY TCAP 10PK INT
Manufacturer Contact
aaholmvej 1-3
osted
lejre, 4320
MDR Report Key13896977
MDR Text Key287905341
Report Number3003442380-2022-00441
Device Sequence Number1
Product Code FPA
Combination Product (y/n)Y
PMA/PMN Number
K032854
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Distributor
Reporter Occupation
Type of Report Initial
Report Date 03/25/2022
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received03/24/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model Number1001681
Device Lot Number5353222
Was Device Available for Evaluation? No Answer Provided
Date Manufacturer Received03/08/2022
Was Device Evaluated by Manufacturer? No Answer Provided

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