FITMORE® HIP STEM, TRIAL RASP, B/6 N/A 01.00559.206

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-03 for FITMORE® HIP STEM, TRIAL RASP, B/6 N/A 01.00559.206 manufactured by Zimmer Gmbh.

Event Text Entries

[116219139] Udi#: (b)(4). Concomitant medical products: associated item number: 00-7806-050-00, item name: sp offset rasp handle 45deg, lot # 63649368. The manufacturer did not receive x-rays, or other source documents for review. The manufacturer received images of the device for review. The manufacturer did not receive the device for investigation. The device history records were reviewed and found to be conforming. Additional information has been requested and is currently not available. 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. Zimmer biomet? S reference number of this file is (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[116219140] It was reported that during the surgery a part of the instrument broke. The surgeon was able to extract the broken part and using another instrument. The case was completed without delay and clinical consequences.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009613350-2018-00754
MDR Report Key7745980
Date Received2018-08-03
Date of Report2018-12-11
Date of Event2018-07-04
Date Mfgr Received2018-11-16
Device Manufacturer Date2008-05-16
Date Added to Maude2018-08-03
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 NameFITMORE® HIP STEM, TRIAL RASP, B/6
Generic NameN/A
Product CodeHTR
Date Received2018-08-03
Model NumberN/A
Catalog Number01.00559.206
Lot Number08.2436375
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZIMMER GMBH
Manufacturer AddressSULZER ALLEE 8 SULZER INDUSTRIE PARK WINTERTHUR 8404 SZ 8404


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-03

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