MAUDE Adverse Event Report: OSTEOMED, LLC BMF FOOTSWITCH

Model Number	450-0390
Medical Device Problem Code	Unintended Electrical Shock (4018)
Health Effect - Clinical Code	Electric Shock (2554)
Date of Event	05/10/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation is on going and a supplemental report will be submitted on completion of investigation.
Event or Problem Description
On (b)(6) 2021 osteomed was notified that, unit (b)(4) and sn (b)(4) was shocking the patients.Per the customer:"we have this unit that is shocking the patients.We seem to think it is the cord because it has a kink in it." on (b)(6) 2021 osteomed reached out to the reporting customer and collected: i spoke with the office manager this morning, who also reported the complaint.She confirmed that there was no patient harm due to the "shocking sensation" that was reported.(harm= burns, cuts, red marks or any injury that would require treatment).The surgeon reported that every time the drill touched the patient there was a sensation that was not reported as painful.To resolve, the surgeon turned off the machine and used another one.There were no delays in surgery to report.Luisa could also not think of any damage to the power console to report.Mdr determination form completed.Based on information reciveved, there is no information that reports any harm to a patient or confirmed malfunction of the product.Complaint determined not to be mdr reportable.On (b)(6) 2021 as a follow up: the customer contacted the sales representative who reported that the customer had experienced a similar sensation with the loaner console and motor that we sent to them in exchange for the units listed on the fer.The customer then investigated the situation further and determined that the sensation was coming from a bad wall receptacle.The wall receptacle has since been repaired and all is well.On (b)(6) 2021 product received at osteomed.And an email was received with a photo of the power console (b)(4), s/n (b)(4).The complaint record was updated and the mdr determination was reviewed.The involved part numbers are as follows: complaint # part # description serial # (b)(4) 450-0005 d-power control console 2i w/irr (b)(4) (b)(4) 450-0084 series ii low profile modular motor unit (b)(4) (b)(4) 450-0390 bmf footswitch -.
Additional Manufacturer Narrative
Corrections: b1, product problem.B4, date of this report (dd-mmm-yyyy) 06-aug-2021.G1, contact office email:(b)(4).H3, device evaluated by manufacturer? [x] not returned to manufacturer.Narrative: the bmf footswitch, part # 450-0390 was not returned.Therefore, no findings and no root cause is available for this specific part.After the occurrence of the event the customer was provided a loaner console (part # 450-0005-01/serial # (b)(6)) and the customer's console (part # 450-0005/serial # (b)(6)) and motor unit (part # 450-0084/serial # (b)(6)) was returned.The returned product was evaluated.The kink in the cable was evaluated and no loss of insulation was identified internally when the cable was opened.Retesting the console to the internal product release testing requirement did not identify any failure that is relevant to this complaint.The console passed all the safety tests per otr-0026 rev.J, (electrical test record--control console assembly, osteopower iii) but failed the irrigation pump functional test.This failure is normal considering that console has not been services for more than 20 years.During the communication with the customer about the failure, the customer stated that the loaner unit exhibited the same issue and "the surgical assistant figured out the problem is that she had the unit plugged into a surge protector and not into a grounded wall socket.After plugging directly to the grounded wall socket the problem was solved.".The caution label clearly stated that grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle marked hospital only or hospital grade.The customer not using a receptacle with a proper grounding is assumed to be the most probable cause for this failure.In light of the complaint an health hazard evaluation (hhe) was initiated to assess the potential hazards.A two-year review did not identify any complaints and ncr related to this issue.The fmea-98019 rev: h for the osteopower system was reviewed and covers the risk of potential shock hazards.The final predicted risk is "low".Based on returned product testing and investigation assessment performed an exact root cause could not be determined, but the most probable cause is the customer not following the labeling and instructions to use a plug with proper grounding.The returned units will be held in quarantine unless/until customer for it to be returned, upon which it will go through normal service process and send back to the customer.This issue will be monitored through routine trending.

• Brand Name: BMF FOOTSWITCH
• Common Device Name: BMF FOOTSWITCH
• Manufacturer (Section D): OSTEOMED, LLC; 3885 arapaho rd.; addison TX 75001
• Manufacturer (Section G): OSTEOMED, LLC; 3885 arapaho rd; addison TX 75001
• Manufacturer Contact: flor rivera ; 3885 arapaho rd.; addison, TX 75001 ; 9726774600
• MDR Report Key: 12310911
• Report Number: 2027754-2021-00011
• Device Sequence Number: 3807078
• Product Code: GBB
• UDI-Device Identifier: 00845694012614
• UDI-Public: 00845694012614
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: 971692
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Administrator/Supervisor
• Remedial Action: Recall
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 08/06/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 450-0390
• Device Catalogue Number: 450-0390
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/03/2021
• Initial Date Received by Manufacturer: 05/10/2021
• Supplement Date Received by Manufacturer: 05/10/2021; 05/10/2021
• Initial Report FDA Received Date: 08/11/2021
• Supplement Report FDA Received Date: 09/10/2021; 11/12/2021
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: 2027754-10/22/21-001-R
• Patient Sequence Number: 1
• Patient Sex: Unknown