ANATOMICAL SHOULDER REVERSE, TRIAL HUMERAL CUP, 0, RETRO N/A 01.04239.600

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-08-06 for ANATOMICAL SHOULDER REVERSE, TRIAL HUMERAL CUP, 0, RETRO N/A 01.04239.600 manufactured by Zimmer Gmbh.

Event Text Entries

[116370606] (b)(4). As no lot number was provided, the device history records could not be reviewed. Pictures and per were received and will be reviewed as part of ongoing investigation. 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


[116370607] It was reported that during the surgical procedure the item has fractured and part of it fell into the patient. The part of the fractured item has been removed from the patient. Attempts to obtain additional information have been made; however, no more is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0009613350-2018-00687
MDR Report Key7751942
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2018-08-06
Date of Report2018-11-13
Date of Event2018-05-21
Date Mfgr Received2018-11-08
Device Manufacturer Date2017-10-16
Date Added to Maude2018-08-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
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 Report3

Device Sequence Number: 0

Brand NameANATOMICAL SHOULDER REVERSE, TRIAL HUMERAL CUP, 0, RETRO
Product CodeHSD
Date Received2018-08-06
Returned To Mfg2018-07-18
Model NumberN/A
Catalog Number01.04239.600
Lot Number4501867130
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No0
Device Event Key0
ManufacturerZIMMER GMBH
Manufacturer AddressSULZER ALLEE 8 SULZER INDUSTRIE PARK WINTERTHUR 8404 SZ 8404

Device Sequence Number: 1

Brand NameANATOMICAL SHOULDER REVERSE, TRIAL HUMERAL CUP, 0, RETRO
Product CodeMJT
Date Received2018-08-06
Returned To Mfg2018-07-18
Model NumberN/A
Catalog Number01.04239.600
Lot Number4501867130
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 2018-08-06

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