SUMMIT INDUSTRIES LLC S210

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-08 for SUMMIT INDUSTRIES LLC S210 manufactured by Summit Industries Llc..

Event Text Entries

[48042218] Shortly thereafter summit replaced the original model s210 table with the same type table so the original one could be returned to the factory to complete the investigation. Upon return of the original table w/ bucky, tests were performed to verify the root cause(s) of the event. Since in this subject case the miswire applied 120vac to the bucky cabinet & then onto the outside metal of the table, which was ungrounded due to the paint barrier & lack of a lockwasher between the power supply & the table base, a shock hazard was present during the installation & resulted in the installer being shocked. In this miswired condition, the bucky would not operate & the installer would not have released the table for use by the end user until the bucky operation was corrected. It is summit's belief that during the installation of a table with a miswired bucky that the installer would clearly notice that the bucky does not operate & would correct the miswire as part of the installation (as happened in this instance). Regarding the likelihood of this electrical shock event reoccurring, please be aware that since 1988, summit has manufactured nearly (b)(4) of these tables (model s210/j005) most of which contain buckys & this is the first & only event of its type during the past 28 years of production. During the past month, as a preventive measure for the present & future, summit has made several design changes to the table to improve grounding continuity & implemented an improved qc test procedure to assure grounding continuity of the table & bucky prior to approval for shipment. In addition, manufacturing personnel were retrained.
Patient Sequence No: 1, Text Type: N, H10


[48042219] On (b)(6) 2016, summit industries technical support received a phone report from an installer (employed by (b)(4)) who observed that during the installation of the radiographic table, model 210, which included a bucky (a bucky is an image receptor cabinet w/ electrically operated reciprocating grid), that the bucky did not operate as received & requested that summit send a part, which was suspected of keeping the bucky from operating properly. The next day ((b)(6) 2016) the installer called back to report that the replacement part did not correct the problem & that while troubleshooting further, a coworker received an electrical shock when he touched the table & related tubestand at the same time. Per the installer, the coworker was not injured & did not require nor receive any medical treatment as a result of the event & neither the installer nor his coworker reported the event to their manager. Subsequent trouble shooting discovered a miswire at the bucky terminal strip which had the 120vac connection reversed with the ground connection. The wiring was corrected & the system was tested & determined to be safe for use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1450503-2016-00001
MDR Report Key5707403
Date Received2016-06-08
Date of Report2016-06-08
Date of Event2016-04-27
Date Mfgr Received2016-04-27
Device Manufacturer Date2016-04-01
Date Added to Maude2016-06-08
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. VILAYETH HUSSAIN
Manufacturer Street2901 WEST LAWRENCE
Manufacturer CityCHICAGO IL 606253621
Manufacturer CountryUS
Manufacturer Postal606253621
Manufacturer Phone7733534030
Manufacturer G1SUMMIT INDUSTRIES LLC
Manufacturer Street2901 WEST LAWERENCE AVENUE
Manufacturer CityCHICAGO IL 606253621
Manufacturer CountryUS
Manufacturer Postal Code606253621
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSUMMIT INDUSTRIES LLC
Generic Name4 WAY FLOAT-TOP TABLE
Product CodeIXQ
Date Received2016-06-08
Returned To Mfg2016-05-17
Model NumberS210
Catalog NumberS210
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSUMMIT INDUSTRIES LLC.
Manufacturer Address2901 WEST LAWRENCE AVENUE CHICAGO IL 606253621 US 606253621


Patients

Patient NumberTreatmentOutcomeDate
10 2016-06-08

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