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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ABBOTT MEDICAL PROCLAIM DRG IMPLANTABLE PULSE GENERATOR; DRG IPG

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ABBOTT MEDICAL PROCLAIM DRG IMPLANTABLE PULSE GENERATOR; DRG IPG Back to Search Results
Model Number 3664
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Pain (1994)
Event Date 04/30/2021
Event Type  Injury  
Manufacturer Narrative
Date of event is estimated.
 
Event Description
It was reported that patient experienced discomfort.As a result, the ipg was explanted and a new device was implanted to avoid additional surgical procedure.There were no complications during the procedure.Patient was stable.
 
Manufacturer Narrative
Based on the information provided a device problem was not identified, as a result a conclusive cause for the reported patient effect, and the relationship to the product, if any, cannot be determined.
 
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Brand Name
PROCLAIM DRG IMPLANTABLE PULSE GENERATOR
Type of Device
DRG IPG
Manufacturer (Section D)
ABBOTT MEDICAL
6901 preston rd
plano TX 75024
MDR Report Key11817460
MDR Text Key250373620
Report Number1627487-2021-13963
Device Sequence Number1
Product Code PMP
UDI-Device Identifier05415067020215
UDI-Public05415067020215
Combination Product (y/n)N
PMA/PMN Number
P150004
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,health
Type of Report Initial,Followup
Report Date 05/23/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date10/04/2019
Device Model Number3664
Device Catalogue Number3664
Device Lot Number6158242
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Initial Date Manufacturer Received 04/30/2021
Initial Date FDA Received05/13/2021
Supplement Dates Manufacturer Received05/20/2021
Supplement Dates FDA Received05/23/2021
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age47 YR
Patient Weight113
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