MAUDE Adverse Event Report: MIO¿; INSET II 46/6 PCC PINK

Lot Number	5187534
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Type of Reportable Event	Malfunction
Event or Problem Description
Unomedical reference number (b)(4).Event occurred in (b)(6).The patient reported that the infusion set tubing detached.The site location was patient's tummy and the pump was in her pocket.There was no stress or pull on the tubing and the pump was not dropped with the set connected to the patient's body.No further information available.

• Brand Name: MIO¿
• Common Device Name: INSET II 46/6 PCC PINK
• MDR Report Key: 8489778
• Report Number: 3003442380-2019-01015
• Device Sequence Number: 11230492
• Product Code: FPA
• UDI-Device Identifier: 05705244007376
• UDI-Public: 05705244007376
• Combination Product (Y/N): N
• PMA/510(K) Number: K160648
• Number of Events Summarized: 1
• 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?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: No Information
• Device Expiration Date: 04/01/2020
• Device Lot Number: 5187534
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/11/2019
• Initial Report FDA Received Date: 04/06/2019
• Patient Sequence Number: 1