MAUDE Adverse Event Report: ZOLL MEDICAL CORPORATION ZOLL PADS-ADULT MULTI-FUNCTION ELECTRODES; PULSE-GENERATOR, PACEMAKER, EXTERNAL

Lot Number 0621A

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Abrasion (1689); Hemorrhage/Bleeding (1888)

Event Date 02/22/2021

Event Type  malfunction  

Event Description

After cardioversion at 200j anterior chest under zoll pad had a perfectly circular excoriated abrasion with minimal bleeding; can see the same shape outline on the zoll pad.Fda safety report id # (b)(4).

• Brand Name: ZOLL PADS-ADULT MULTI-FUNCTION ELECTRODES
• Type of Device: PULSE-GENERATOR, PACEMAKER, EXTERNAL
• Manufacturer (Section D): ZOLL MEDICAL CORPORATION
• MDR Report Key: 11602761
• MDR Text Key: 243642590
• Report Number: MW5100483
• Device Sequence Number: 1
• Product Code: DTE
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date: 03/30/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/31/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 02/06/2022
• Device Lot Number: 0621A
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was Device Evaluated by Manufacturer?: No Information
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Age: 69 YR
• Patient Weight: 81