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 2018-12-07 for AUTOCLAVABLE INTERNAL HANDLES 8011-0501-01 8011050101 manufactured by Zoll Medical Corporation.

Event Text Entries

[129632037] Zoll medical corporation has received the product and will be providing a supplemental report when our investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


[129632038] Complainant alleged that during biomed testing, the device's defib output was out of specification. Complainant indicated that there was no patient involvement in the reported malfunction.
Patient Sequence No: 1, Text Type: D, B5


[131727698] The device was evaluated by zoll medical (b)(4). The reported problem was observed during testing. The discharge values were out of range. The autoclavable handle was sent to zoll medical (b)(4) for evaluation. Evaluation of autoclavable handle could not duplicate the reported malfunction. The handle was scrapped. Analysis of reports of this type has not identified an increase in trend.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1220908-2018-03558
MDR Report Key8142399
Report SourceFOREIGN
Date Received2018-12-07
Date of Report2018-11-16
Date Mfgr Received2018-11-16
Device Manufacturer Date2017-06-01
Date Added to Maude2018-12-07
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 Received2018-12-07
Returned To Mfg2018-12-04
Model Number8011-0501-01
Catalog Number8011050101
Lot NumberNA
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZOLL MEDICAL CORPORATION
Manufacturer Address269 MILL ROAD CHELMSFORD MA 01824 US 01824


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-07

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