AUTOCLAVABLE INTERNAL HANDLES 8011-0501-01 8011050101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2018-09-06 for AUTOCLAVABLE INTERNAL HANDLES 8011-0501-01 8011050101 manufactured by Zoll Medical Corporation.

Event Text Entries

[119436779] Zoll medical corporation has not received the product for evaluation and this complaint is still under investigation.
Patient Sequence No: 1, Text Type: N, H10


[119436780] Complainant alleged that during biomed testing, the associated defibrillator failed to discharge using these attached internal handles. Complainant indicated that there was no patient involvement in the reported malfunction.
Patient Sequence No: 1, Text Type: D, B5


[123714644] The internal handles were returned to zoll medical corporation for evaluation. During testing of the internal handles with a simulator, the device did not shock when the shock button on the internal handle was pressed. The malfunction was duplicated and attributed to a faulty discharge button on the paddle. The internal handles were scrapped. Analysis for reports of this type has not identified an increase in trend
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1220908-2018-02540
MDR Report Key7851738
Report SourceFOREIGN
Date Received2018-09-06
Date of Report2018-08-16
Date Mfgr Received2018-08-16
Device Manufacturer Date2016-10-01
Date Added to Maude2018-09-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer Street269 MILL ROAD
Manufacturer CityCHELMSFORD MA 01824
Manufacturer CountryUS
Manufacturer Postal01824
Manufacturer Phone9784219552
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAUTOCLAVABLE INTERNAL HANDLES
Generic NameINTERNAL PADDLE
Product CodeLDD
Date Received2018-09-06
Returned To Mfg2018-09-04
Model Number8011-0501-01
Catalog Number8011050101
Lot NumberNA
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZOLL MEDICAL CORPORATION
Manufacturer Address269 MILL ROAD CHELMSFORD MA 01824 US 01824


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.