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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL, INC. DISPOSABLE GROUNDING PAD W/OUT CABLE; PROBE, RADIOFREQUENCY LESION
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ST. JUDE MEDICAL, INC. DISPOSABLE GROUNDING PAD W/OUT CABLE; PROBE, RADIOFREQUENCY LESION Back to Search Results
Model Number RF-DGP-L
Medical Device Problem Code Material Deformation (2976)
Health Effect - Clinical Code Irritation (1941)
Date of Event 05/10/2019
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
One disposable grounding pad without cable was returned for investigation.A clear film was noted on the surface of the grounding pad.Further investigation revealed the grounding pad was assembled with the clear film on the inside layer of the blue liner.
 
Event or Problem Description
This report is to advise of an event during analysis confirming the clear film of the grounding pad was assembled on the inside layer of the blue liner.
 
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Brand Name
DISPOSABLE GROUNDING PAD W/OUT CABLE
Common Device Name
PROBE, RADIOFREQUENCY LESION
Manufacturer (Section D)
ST. JUDE MEDICAL, INC.
14901 deveau place
minnetonka MN 55345
MDR Report Key8958527
Report Number2182269-2019-00156
Device Sequence Number19444111
Product Code GXD
UDI-Device Identifier05415067023612
UDI-Public05415067023612
Combination Product (Y/N)N
Initial Reporter StateKY
Initial Reporter CountryUS
PMA/510(K) Number
K111576
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Other Health Care Professional
Remedial Action Recall
Type of Report Initial,Followup
Report Date (Section B) 10/18/2019
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 Health Professional
Device Model NumberRF-DGP-L
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer07/01/2019
Was the Report Sent to FDA? No
Initial Date Received by Manufacturer 08/09/2019
Supplement Date Received by Manufacturer10/14/2019
Initial Report FDA Received Date09/03/2019
Supplement Report FDA Received Date10/18/2019
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
If action reported to FDA under 21 USC 360i(g), list
FDA-assigned Recall Number or include a statement		FA-Q419-NM_EP-1
Patient Sequence Number1
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