EKSO NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,health professional report with the FDA on 2015-09-02 for EKSO NA manufactured by Ekso Bionics, Inc..

Event Text Entries

[25232342] Device was returned to manufacturer for evaluation and was retained. Manufacturer determined that fasteners sheared under bending stresses greater than the fatigue load of the fastener causing the foot plate to partially separate from the ankle. Failure mode of fasteners was from bending fatigue; however root cause analysis of failure mode is still under investigation and results are pending completion of evaluation. Additional info follow-up will be submitted when the following info becomes available: mdr submitted via paper on deadline date instead of digitally via webtrader since production account is still pending activation. (d2b) this is currently registered under procode bxb as indicated in (d2b). This device is currently pending 510(k) approval under procode phl. Results and conclusion - as root cause analysis is still pending evaluation. Remedial action - root cause analysis is still pending evaluation.
Patient Sequence No: 1, Text Type: N, H10


[25232343] [device #2 similar to mdr 3009495988-2015-00001]. During physical therapy session, physical therapist noticed that the pt's hips would rotate and drop bit during the loading phase for a few steps, which was not normal. The physical therapist put the device into a chair. Upon inspection of the device, the physical therapist noticed that the foot plate became partially separated from the rest of the ankle, allowing the foot plate to rotate out of position. The pt was safely removed from the device and sustained no injuries and no medical follow-up or intervention was needed. No physical therapists, therapists, or third persons have been affected or injured.
Patient Sequence No: 1, Text Type: D, B5


[40348666] Root cause was under-torqued (preload) fasteners and loss of joint tension due to the degenerative compression of the carbon fiber footplate. Remedial action: a bearing plate will be placed between the carbon fiber footplate and ankle box, and washers will be placed under the fasteners along with thread locker. Since this failure mode represents a low risk of injury the corrective actions will be made at the next routine service period.
Patient Sequence No: 1, Text Type: N, H10


[40348667] This event did not lead to an injury and there have been no injuries reported since the mdr was filed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009495988-2015-00003
MDR Report Key5057620
Report SourceCONSUMER,HEALTH PROFESSIONAL
Date Received2015-09-02
Date of Report2015-09-02
Date of Event2015-08-03
Date Mfgr Received2015-08-05
Device Manufacturer Date2012-03-01
Date Added to Maude2015-09-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
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. DOUG HUMPHREY
Manufacturer Street1414 HARBOUR WAY S SUITE 1201
Manufacturer CityRICHMOND CA 94804
Manufacturer CountryUS
Manufacturer Postal94804
Manufacturer Phone5109841761
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameEKSO
Generic NameEKSO
Product CodePHL
Date Received2015-09-02
Returned To Mfg2015-08-05
Model NumberEKSO
Catalog NumberNA
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No0
Device Event Key0
ManufacturerEKSO BIONICS, INC.
Manufacturer AddressRICHMOND CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2015-09-02

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