MAUDE Adverse Event Report: AUTOSOFT 90; INSET II 2-PACK 60/6 GREY TCAP

Model Number 1000281

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) 2021, the patient's infusion set's tubing detached/broken at the site connector back-to-back with two infusion sets.Therefore, her blood glucose level was 314 mg/dl at the time of the event.The infusion set had been used for about an hour.Moreover, they replaced the infusion set and insulin was resumed successfully.No further information available.

• Brand Name: AUTOSOFT 90
• Type of Device: INSET II 2-PACK 60/6 GREY TCAP
• Manufacturer Contact: aaholmvej 1-3; osted; lejre, 4320
• MDR Report Key: 12914918
• MDR Text Key: 281583716
• Report Number: 3003442380-2021-00771
• Device Sequence Number: 1
• Product Code: FPA
• UDI-Device Identifier: 05705244014541
• UDI-Public: 05705244014541
• Combination Product (y/n): Y
• PMA/PMN Number: K032854
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Distributor
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 12/02/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/02/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 1000281
• Device Lot Number: UNKNOWN
• Date Manufacturer Received: 11/24/2021
• Patient Sequence Number: 1