BMP SLEEVE GRIP CRIMPER N/A 498003

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2018-02-08 for BMP SLEEVE GRIP CRIMPER N/A 498003 manufactured by Zimmer Biomet, Inc..

Event Text Entries

[99912729] (b)(4) (b)(6). Customer has indicated that the product is in process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[99912730] It was reported that during use, the tip of the instrument broke; however, the surgery took place normally. No adverse events have been reported as a result of the malfunction. Attempts have been made and additional information on the reported event is unavailable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001825034-2018-00402
MDR Report Key7252512
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2018-02-08
Date of Report2018-06-19
Date of Event2017-12-01
Date Mfgr Received2018-06-18
Device Manufacturer Date2016-12-01
Date Added to Maude2018-02-08
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 BIOMET, INC.
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameBMP SLEEVE GRIP CRIMPER
Generic NameCRIMPER, PIN
Product CodeHXQ
Date Received2018-02-08
Returned To Mfg2018-03-23
Model NumberN/A
Catalog Number498003
Lot Number336650
ID Number(01) 00880304009608
OperatorPHYSICIAN
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-08

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