RESPONSE LARGE SET SCREW N/A 00-1003-4001

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 2019-05-01 for RESPONSE LARGE SET SCREW N/A 00-1003-4001 manufactured by Orthopediatrics, Inc.

Event Text Entries

[143754574] Reference: (b)(4). Customer has indicated that the product is in process of being returned to orthopediatrics for investigation. Once the investigation has been completed, a follow-up mdr will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[143754575] It was reported that following a posterior fusion surgery, the patient experienced back pain and clicking. It was discovered during the revision procedure that a set screw was loose. No additional patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006460162-2019-00015
MDR Report Key8571189
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2019-05-01
Date of Report2019-05-01
Date of Event2019-03-25
Date Mfgr Received2019-04-01
Device Manufacturer Date2016-05-16
Date Added to Maude2019-05-01
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 ContactLEIGH JESSOP
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5742670872
Manufacturer G1ORTHOPEDIATRICS, INC
Manufacturer Street2850 FRONTIER DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRESPONSE LARGE SET SCREW
Generic NamePEDICLE SCREW SPINAL SYSTEM
Product CodeOSH
Date Received2019-05-01
Model NumberN/A
Catalog Number00-1003-4001
Lot NumberM69067-B
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerORTHOPEDIATRICS, INC
Manufacturer Address2850 FRONTIER DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-05-01

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