MAUDE Adverse Event Report: MEDTRONIC MINIMED MEDTRONIC GUARDIAN SENSOR (3); SENSOR, GLUCOSE, INVASIVE

Model Number	MMT-7020A
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	02/28/2021
Type of Reportable Event	Malfunction
Event or Problem Description
Inserted new medtronic guardian sensor (3) in the morning and about 5 hours later i had to replace the sensor due to sensor failure.Fda safety report id # (b)(4).

• Brand Name: MEDTRONIC GUARDIAN SENSOR (3)
• Common Device Name: SENSOR, GLUCOSE, INVASIVE
• Manufacturer (Section D): MEDTRONIC MINIMED
• MDR Report Key: 11404365
• Report Number: MW5099752
• Device Sequence Number: 4053452
• Product Code: MDS
• UDI-Device Identifier: 20763000337005
• UDI-Public: 20763000337005
• Initial Reporter State: OH
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Voluntary
• Initial Reporter Occupation: Patient
• Type of Report: Initial
• Report Date (Section B): 02/28/2021

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: 01/15/2022
• Device Model Number: MMT-7020A
• Device Catalogue Number: G12260-18
• Device Lot Number: HG50LUF
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 03/02/2021
• Patient Sequence Number: 1
• Patient Age: 53 YR
• Patient Weight: 86