ARTICULATING DISTRACTOR 202718200

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-19 for ARTICULATING DISTRACTOR 202718200 manufactured by Depuy Spine Inc.

Event Text Entries

[125441893] (b)(4). A complaint investigation will be performed. The complaint product is not available for the investigation. A supplemental report is not anticipated unless the results of the complaint investigation identify a corrective action or additional relevant information. Should the product become available, a physical evaluation will be conducted and a supplemental report filed with the results. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10


[125441894] It was reported that the spreader came apart in sterilization, pieces missing needing full replacement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1526439-2018-50999
MDR Report Key7986532
Date Received2018-10-19
Date of Report2018-10-02
Date of Event2018-10-01
Date Mfgr Received2018-10-02
Date Added to Maude2018-10-19
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 ContactJASON BUSCH
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone5088808100
Manufacturer G1DEPUY SPINE INC
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal Code02767
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameARTICULATING DISTRACTOR
Generic NameDISSECTOR, SURGICAL, GENERAL & PLASTIC SURGERY
Product CodeGDI
Date Received2018-10-19
Model Number202718200
Catalog Number202718200
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY SPINE INC
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-19

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