BIOMET EBI BONE HEALING SYSTEM N/A 1068234

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-01-02 for BIOMET EBI BONE HEALING SYSTEM N/A 1068234 manufactured by Ebi, Llc..

Event Text Entries

[177361897] (b)(4). Date of event: the event occurred sometime in (b)(6) 2019. The customer has indicated that the product is in the process of being returned to zimmer biomet for investigation. Once the investigation has been completed, a follow-up mdr will be submitted. The device has not been returned.
Patient Sequence No: 1, Text Type: N, H10


[177361898] It was reported that the patient was experiencing pain from the bone healing system (bhs). The patient used the bhs unit 5-6 times and stated that she experienced stabbing pains. The patient did contact their doctor and was advised to stop using the bhs. No additional patient consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002242816-2020-00001
MDR Report Key9539838
Report SourceCONSUMER
Date Received2020-01-02
Date of Report2020-01-02
Date Mfgr Received2019-12-23
Date Added to Maude2020-01-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSARA DAILEY
Manufacturer Street399 JEFFERSON ROAD
Manufacturer CityPARSIPPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal07054
Manufacturer Phone9732999300
Manufacturer G1EBI, LLC.
Manufacturer Street399 JEFFERSON ROAD
Manufacturer CityPARSIPPANY NJ 07054
Manufacturer CountryUS
Manufacturer Postal Code07054
Single Use3
Previous Use Code3
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameBIOMET EBI BONE HEALING SYSTEM
Generic NameSTIMULATOR, BONE GROWTH, NON-INVASIVE
Product CodeLOF
Date Received2020-01-02
Model NumberN/A
Catalog Number1068234
Lot NumberN/A
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEBI, LLC.
Manufacturer Address399 JEFFERSON ROAD PARSIPPANY NJ 07054 US 07054


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-02

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