MIS, RASP HANDLE, DOUBLE OFFSET, LEFT N/A 01.00001.003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-23 for MIS, RASP HANDLE, DOUBLE OFFSET, LEFT N/A 01.00001.003 manufactured by Zimmer Gmbh.

Event Text Entries

[124811503] (b)(4). The manufacturer did not receive x-rays, or other source documents for review. The manufacturer did not receive the device yet, however it is indicated by complainant that it will be returned for investigation. The device manufacturing quality records indicate that the released components met all requirements to perform as intended. A cause for this specific event cannot be ascertained from the information provided. As soon as supplemental information becomes available an updated report will be submitted. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[124811504] It was reported that the mis, rasp handle, double offset, left broke (locking mechanism loosened while hammering) during a surgery. The implantation and explantation dates are left empty as the device involved in this complaint is an instrument. Hence, no expiration date is captured, for the same reason.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009613350-2018-01092
MDR Report Key7994174
Date Received2018-10-23
Date of Report2019-02-12
Date of Event2018-09-28
Date Mfgr Received2019-02-08
Device Manufacturer Date2012-10-22
Date Added to Maude2018-10-23
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 ContactMS. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER GMBH
Manufacturer StreetSULZER ALLEE 8 SULZER INDUSTRIE PARK
Manufacturer CityWINTERTHUR 8404
Manufacturer CountrySZ
Manufacturer Postal Code8404
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report0

Device Details

Brand NameMIS, RASP HANDLE, DOUBLE OFFSET, LEFT
Generic NameN/A
Product CodeHAO
Date Received2018-10-23
Returned To Mfg2018-11-07
Model NumberN/A
Catalog Number01.00001.003
Lot Number12.769821
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER GMBH
Manufacturer AddressSULZER ALLEE 8 SULZER INDUSTRIE PARK WINTERTHUR 8404 SZ 8404


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-23

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