DIGIT WIDGET DWD-232

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-06 for DIGIT WIDGET DWD-232 manufactured by Hand Biomechanics Lab, Inc..

Event Text Entries

[178001203] Analyzed production records, performed historical data analysis and trend analysis. No trend related to probable irradiation dose lots or device lots were noted. Confirmed labeling included cautions regarding pin site care.
Patient Sequence No: 1, Text Type: N, H10


[178001204] Patient had surgery to install a digit widget external fixation system. A hand physical therapist reported 2 weeks post operative that the patient was being treated with oral antibiotic for a possible pin tract infection.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2919128-2020-00002
MDR Report Key9676912
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-06
Date of Report2020-02-06
Date Mfgr Received2020-01-06
Device Manufacturer Date2019-02-14
Date Added to Maude2020-02-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DUSTIN DEQUINE
Manufacturer Street77 SCRIPPS DRIVE, SUITE 104
Manufacturer CitySACRAMENTO CA 95825
Manufacturer CountryUS
Manufacturer Postal95825
Manufacturer Phone9169235073
Manufacturer G1HAND BIOMECHANICS LAB, INC.
Manufacturer Street77 SCRIPPS DRIVE, SUITE 104
Manufacturer CitySACRAMENTO CA 95825
Manufacturer CountryUS
Manufacturer Postal Code95825
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDIGIT WIDGET
Generic NameDIGIT WIDGET
Product CodeJDW
Date Received2020-02-06
Model NumberDWD-232
Catalog NumberDWD-232
Lot NumberDWD-118-178A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHAND BIOMECHANICS LAB, INC.
Manufacturer Address77 SCRIPPS DRIVE, SUITE 104 SACRAMENTO CA 95825 US 95825


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-06

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