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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC PUERTO RICO OPERATIONS CO. RESERVOIR 3ML MMT-332A; PUMP, INFUSION

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MEDTRONIC PUERTO RICO OPERATIONS CO. RESERVOIR 3ML MMT-332A; PUMP, INFUSION Back to Search Results
Model Number MMT-332A
Device Problem Air Leak (1008)
Patient Problem Hyperglycemia (1905)
Event Date 05/30/2018
Event Type  malfunction  
Manufacturer Narrative
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 call that reservoir had air bubbles.Customer¿s blood glucose level was 265 mg/dl at the time of incident.Approximate size of air bubbles is small that conglomerate into bigger ones.The reservoir will not be returned for analysis.
 
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Brand Name
RESERVOIR 3ML MMT-332A
Type of Device
PUMP, INFUSION
Manufacturer (Section D)
MEDTRONIC PUERTO RICO OPERATIONS CO.
ceiba norte ind. park #50 road
juncos 00777 -386
Manufacturer (Section G)
MEDTRONIC PUERTO RICO OPERATIONS CO.
ceiba norte ind. park #50 road
juncos 00777 -386
Manufacturer Contact
gerwin de graaff
ceiba norte ind. park #50 road
juncos 00777--386
MDR Report Key7649749
MDR Text Key112870701
Report Number3004209178-2018-86568
Device Sequence Number0
Product Code FRN
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Patient
Type of Report Initial
Report Date 06/29/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/29/2018
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberMMT-332A
Device Catalogue NumberMMT-332A
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received05/30/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Age70 YR
Patient Weight180
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