MAUDE Adverse Event Report: EBI, LLC. BIOMET SPINALPAK / ORTHOPAK; ELECTRODE, CUTANEOUS

Model Number	106130-20
Medical Device Problem Code	Patient-Device Incompatibility (2682)
Health Effect - Clinical Codes	Itching Sensation (1943); Skin Inflammation/ Irritation (4545)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Section b3: as the date of the event is unknown, the event date is estimated as january of 2026.
Event or Problem Description
It was reported by the sales representative (b)(6) that the patient had a skin irritation with 72r electrodes.The customer service representative called the patient to collect details and had to leave a voicemail for a return call.The patient called back and advised the irritation started weeks ago on (b)(6) 2025.The patient saw her doctor regarding the irritation and the doctor told her to reduce the time to 30 minutes and then gradually increase the time.By this time the patient has stopped using the spak after following the doctor's instructions the itching and redness was too much.And she could not do it.The patient cleans the area with alcohol and tried again.The patient started itching within an hour.The patient has sensitive skin.The electrodes were used at least 3 or 4 times before changing them.The patient removed the electrodes when she took a shower.The skin was red and itchy.No welts or blisters.The area was cleaned with soap and water one day she used alcohol.The patient did not apply anything on the area.The patient has food allergies and seasonal allergies.A pcp prescribed a cream.The patient was not home to offer the name of the cream.The patient will perform the time test with the 63b electrodes.A replacement supply of 63b electrodes was shipped to the patient's home.A pouch was shipped for product return.
Event or Problem Description
It was reported by the sales representative (b)(6) that the patient had a skin irritation with 72r electrodes.The customer service representative called the patient to collect details and had to leave a voicemail for a return call.The patient called back and advised the irritation started weeks ago on (b)(6) 2025.The patient saw her doctor regarding the irritation and the doctor told her to reduce the time to 30 minutes and then gradually increase the time.By this time the patient has stopped using the spak after following the doctor's instructions the itching and redness was too much.And she could not do it.The patient cleans the area with alcohol and tried again.The patient started itching within an hour.The patient has sensitive skin.The electrodes were used at least 3 or 4 times before changing them.The patient removed the electrodes when she took a shower.The skin was red and itchy.No welts or blisters.The area was cleaned with soap and water one day she used alcohol.The patient did not apply anything on the area.The patient has food allergies and seasonal allergies.A pcp prescribed a cream.The patient was not home to offer the name of the cream.The patient will perform the time test with the 63b electrodes.A replacement supply of 63b electrodes was shipped to the patient's home.A pouch was shipped for product return.
Additional Manufacturer Narrative
Additional information - b4: date of this report, d8: device available for evaluation, d9: returned to manufacturer date.G3: date received by manufacturer.A visual inspection of the customer returned product was performed.Included was 1 pack of 72r electrodes part no.106130-20 with lot no.25f002 received in a shipping mailer cushion envelope.The parts received look to be in good condition from the visual/cosmetic view.The certificate of conformance was requested and reviewed in the product information section and there were no non-conformances or deviations reported.The 72r electrodes were received for evaluation.The certificate of conformance was reviewed in the product information section.All evaluation results are included in the summary section.Review of complaint history identified 164 total complaints from (jan 5, 2025) to (jan 5, 2026) for pn (106130-20) and events related to (electrode irritation/rash).Keyword search criteria: (complaint codes: electrode: irritation, electrode: rash).The search was specified to the lot no.25f002.The search identified (3) complaint.Review of the information provided by the customer and along with findings from the investigation, indicate there are no systemic issues with the product or lot.Therefore, the bill of materials (boms), material certifications, master labels, and product drawings were not requested or pulled during this investigation.The approved suppliers were not contacted, and the product was not pulled from stock for evaluation.No physical and/or functional condition could be found after review of the certificate of conformance that could be considered a causal factor for the reported complaint.The reported claim could be associated with a side effect/clinical condition of the patient which is unknown.The reported condition is related to clinical factors beyond the scope of the device investigation covered in the complaint investigation as part of the manufacturing review.Therefore, no further actions are required at this time.Ebi will continue to monitor for trends.This device is used for treatment.A follow-up report will be sent if additional information is obtained that adds value to the relevant content of this report.

• Brand Name: BIOMET SPINALPAK / ORTHOPAK
• Common Device Name: ELECTRODE, CUTANEOUS
• Manufacturer (Section D): EBI, LLC.; 1 gatehall dr; suite 303; parsippany NJ 07054
• Manufacturer (Section G): EBI, LLC; 1 gatehall dr; suite 303; parsippany NJ 07054
• Manufacturer Contact: stephanie smith ; 1 gatehall dr; suite 303; parsippany, NJ 07054 ; 9732999300
• MDR Report Key: 24183765
• Report Number: 0002242816-2026-00006
• Device Sequence Number: 10016926
• Product Code: GXY
• UDI-Device Identifier: 00812301020201
• UDI-Public: 00812301020201
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: P850022
• Exemption Number: 5645646
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 03/19/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Lay User/Patient
• Device Model Number: 106130-20
• Device Catalogue Number: 106130-20
• Device Lot Number: 25F002
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/21/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/26/2026
• Supplement Report FDA Received Date: 03/19/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/20/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 82 YR
• Patient Sex: Female
• Patient Ethnicity: Non Hispanic