MAUDE Adverse Event Report: ZOLL MEDICAL CORPORATION ASSY, PADDLES, ENG; MSERIES PADDLES

Model Number 1001-001150-01

Device Problem Defibrillation/Stimulation Problem (1573)

Patient Problem No Patient Involvement (2645)

Event Type  malfunction  

Manufacturer Narrative

Zoll medical corporation has not received the product for evaluation and this complaint is still under investigation.

Event Description

Complainant alleged that during incoming testing, the device caused the associated defibrillator to display a "release button" message using these external paddles.Complainant indicated that there was no patient involvement in the reported malfunction.

Manufacturer Narrative

The customer was contacted for return of the suspect product.The product has not been returned to zoll for evaluation.

• Brand Name: ASSY, PADDLES, ENG
• Type of Device: MSERIES PADDLES
• Manufacturer (Section D): ZOLL MEDICAL CORPORATION; 269 mill road; chelmsford MA 01824
• Manufacturer Contact: 269 mill road; chelmsford, MA 01824 ; 9784219552
• MDR Report Key: 7797593
• MDR Text Key: 117603682
• Report Number: 1220908-2018-02333
• Device Sequence Number: 1
• Product Code: LDD
• UDI-Device Identifier: 00847946023010
• UDI-Public: 00847946023010
• Combination Product (y/n): N
• Reporter Country Code: ID
• PMA/PMN Number: K972241
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 07/30/2018

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
• Device Operator: Other
• Device Model Number: 1001-001150-01
• Device Catalogue Number: 1001-001150-01
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 07/30/2018
• Initial Date FDA Received: 08/20/2018
• Supplement Dates Manufacturer Received: 07/30/2018
• Supplement Dates FDA Received: 09/10/2018
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 12/01/2015
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1