MAUDE Adverse Event Report: BIO-DETEK INCORPORATED CPR-D PADZ; ELECTRODE

Model Number	8900-0800-01
Medical Device Problem Code	Failure of Device to Self-Test (2937)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Zoll medical corporation has not received the product for evaluation and this complaint is still under investigation.
Event or Problem Description
Complainant alleged that during a routine shift check by a clinician, the associated device prompted a "unit failed" message using these cpr-d padz.Complainant indicated that there was no patient involvement in the reported malfunction.
Additional Manufacturer Narrative
The cpr-d padz were returned to zoll medical corporation for evaluation.The customer's report of unit failed in rescue mode was not replicated or confirmed.The cpr-d padz were tested with a test r series device and it displayed cpr puck related alerts which would not prevent the pads from being able to be used in a rescue.The pads were scrapped after testing.Replacement pads were sent to the customer.Analysis of reports of this type has not identified an increase in trend.

• Brand Name: CPR-D PADZ
• Common Device Name: ELECTRODE
• Manufacturer (Section D): BIO-DETEK INCORPORATED; 525 narragansett park drive; pawtucket RI 02861
• Manufacturer Contact: tina lombari ; 525 narragansett park drive; pawtucket, RI 02861 ; 4017291400
• MDR Report Key: 21284005
• Report Number: 1218058-2025-00007
• Device Sequence Number: 20791202
• Product Code: MKJ
• UDI-Device Identifier: 00847946000189
• UDI-Public: (01)00847946000189(17)280909(10)2423A
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: P160022
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/10/2025

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: Other
• Device Model Number: 8900-0800-01
• Device Lot Number: 2423A
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/10/2025
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/31/2025
• Supplement Report FDA Received Date: 03/30/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/11/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown