MAUDE Adverse Event Report: MEDTRONIC MINIMED INFST MMT-905T MIO 2PK 13MM23N; SET, ADMINISTRATION, INTRAVASCULAR

Model Number MMT-905T

Device Problems Bent (1059); Failure to Deliver (2338); Device Displays Incorrect Message (2591)

Patient Problem Irritation (1941)

Event Date 03/04/2017

Event Type  malfunction  

Manufacturer Narrative

Note: this is a remediation mdr.Medtronic diabetes implemented revised mdr reportability criteria effective on october 1, 2017.Subsequently, medtronic diabetes conducted a two year retrospective review of complaints.This event was retrospectively identified to be reportable based on the revised mdr reportability criteria.Currently it is unknown whether or not the device may have caused or contributed to the event as no product has been returned.No conclusion can be drawn at this time.We therefore consider this report complete to the best of our knowledge.

Event Description

Customer reported via phone call that they received a no delivery alarm that was resolved by changing their infusion set.The customer's blood glucose level at the time of the incident was 9.1 mmol/l.Customer was able to troubleshoot at the time of the call.The infusion set cannula was bent upon removal.Customer reported red irritation, blood and pain at the infusion set insertion site.The infusion set is not expected to be returned.

• Brand Name: INFST MMT-905T MIO 2PK 13MM23N
• Type of Device: SET, ADMINISTRATION, INTRAVASCULAR
• Manufacturer (Section D): MEDTRONIC MINIMED; 18000 devonshire st.; northridge CA 91325 1219
• Manufacturer (Section G): MEDTRONIC MINIMED; 18000 devonshire st.; northridge CA 91325 1219
• Manufacturer Contact: gerwin de graaff ; 18000 devonshire st.; northridge, CA 91325-1219
• MDR Report Key: 7251889
• MDR Text Key: 99800698
• Report Number: 2032227-2018-01344
• Device Sequence Number: 1
• Product Code: FPA
• UDI-Device Identifier: 20643169668359
• UDI-Public: (01)20643169668359(017)20190201
• Combination Product (y/n): N
• Reporter Country Code: CA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 02/08/2018

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
• Device Operator: Lay User/Patient
• Device Expiration Date: 02/01/2019
• Device Model Number: MMT-905T
• Device Catalogue Number: MMT-905T
• Device Lot Number: 5136899
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 03/04/2017
• Initial Date FDA Received: 02/08/2018
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1