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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC PUERTO RICO OPERATIONS CO. PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP MMT-723NAS; PUMP, INFUSION, INSULIN, TO BE USED WITH INVASIVE GLUCOSE SENSOR

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MEDTRONIC PUERTO RICO OPERATIONS CO. PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP MMT-723NAS; PUMP, INFUSION, INSULIN, TO BE USED WITH INVASIVE GLUCOSE SENSOR Back to Search Results
Model Number MMT-723NAS
Medical Device Problem Code Moisture or Humidity Problem (2986)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 06/07/2018
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
This mdr related to the puerto rico manufacturing site has been assigned a medwatch number from the medtronic minimed northridge site, per variance 5.Pump passed the displacement test and self test.However, moisture damage at electronic assembly.Also, moisture damage motor during visual inspection.The following were noted during visual inspection: cracked battery tube threads, missing end cap sticker, stained address/serial number label and broken reservoir tube lip.The pump was received with 10% of reservoir tube lip broken off, however the test infusion set and reservoir did lock properly into place.Moisture damaged was confirmed on a electronic.Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employees caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
 
Event or Problem Description
It was reported to medtronic minimed that the customer reported moisture damage to pump.The customer reported no adverse event.The event involved product mmt-723nas.Troubleshooting was performed and issue was unresolved.No harm requiring medical intervention was reported.Product return was requested for mmt-723nas and insulin pump was retuned for analysis.
 
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Brand Name
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP MMT-723NAS
Common Device Name
PUMP, INFUSION, INSULIN, TO BE USED WITH INVASIVE GLUCOSE SENSOR
Manufacturer (Section D)
MEDTRONIC PUERTO RICO OPERATIONS CO.
ceiba norte ind. park #50 road
juncos 00777 -386
*  00777-3869
Manufacturer (Section G)
MEDTRONIC PUERTO RICO OPERATIONS CO.
ceiba norte ind. park #50 road
juncos 00777 -386
*   00777-3869
Manufacturer Contact
lusine boyadzhyan
ceiba norte ind. park #50 road
juncos 00777--386
*   00777-3869
MDR Report Key20458957
Report Number2032227-2024-254687
Device Sequence Number15383240
Product Code OYC
UDI-Device Identifier00643169507258
UDI-Public(01)00643169507258
Combination Product (Y/N)N
Initial Reporter StateNC
Initial Reporter CountryUS
PMA/510(K) Number
P150019
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Consumer
Initial Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date (Section B) 10/16/2024
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 Lay User/Patient
Device Model NumberMMT-723NAS
Device Catalogue NumberMMT-723NAS
Device Lot NumberB5723NASJ
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer09/09/2024
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 09/26/2024
Initial Report FDA Received Date10/16/2024
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured09/29/2016
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device A
Patient Sequence Number1
Patient Age46 YR
Patient SexMale
Patient Weight93 KG
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