BIOLOX DELTA CERAMIC HEADS 36MM 12-115121

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-25 for BIOLOX DELTA CERAMIC HEADS 36MM 12-115121 manufactured by Biomet, Inc..

Event Text Entries

[134135308] Excerpts from surgeon's operative note: final stem placed in the proximal femur and seated. Cleansed the femoral trunnion and impacted the final ceramic head onto the femoral trunnion. As we did this it appeared to have solid cold weld. I went to reduce the hip and when i placed my finger on the femoral head i realized that there was a crack within the femoral head. Then externally rotated the hip again and realized that the femoral head ceramic head fractured. The anterior two-thirds of this head was cold welded to the femoral trunnion and the posterior one third had a loose fragment. There were several other fragments noted. We removed all fragments that we could identify. I actually had to use a square-ended impactor to dislodge the anterior two-thirds of the ceramic head from the femoral trunnion. I "place" lighted retractors in and around the acetabulum and we checked the acetabular liner and soft tissue for any further debris. There was no marking or scoring of the polyethylene liner. There were 2 fragments of ceramic head that were removed. We tried to reconstruct the ceramic femoral head on the back table and it appeared that we had all fragments. I utilized fluoroscopic guidance and no further fragments of ceramic were identified. We irrigated the wound with sterile normal saline 3 l. I again placed retractors and looked for any further fragments and none were found. Cleansed and dried the femoral trunnion; there was no deformity of the femoral trunnion identified. The biolox option ceramic femoral head with a +3 mm neck length was then impacted onto the femoral trunnion with solid cold fit. No fractures of this component were noted. We again checked the acetabulum for debris and none was found. We reduced the hip and again tested for stability and it was found stable. Post op x-ray taken in pacu revealed a retained foreign body. Patient was informed & returned to surgery. Excerpt from surgeon's 2nd operative note: fluoroscopic guidance; we rotated the hip and under a rotation view you could see that there was a small fragment radiopaque next to the femoral trunnion. Looked down into the joint and evacuated hematoma. I could not see this fragment of ceramic and had to utilize fluoroscopy to identify it. I was then able to remove it utilizing a pituitary roger. Irrigated the hip with sterile normal saline. We took multiple fluoroscopic images of the hip in multiple planes and did not see any further radiopaque material foreign body. The wound was copiously lavaged with sterile normal saline. Patient was discharged without further incident. Manufacturer response for 12-115121 modular ceramic head, metal on polyethylene, 36mm, (brand not provided) (per site reporter). Manufacturer wishes to take possession of the device for testing and evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8276997
MDR Report Key8276997
Date Received2019-01-25
Date of Report2019-01-24
Date of Event2019-01-14
Report Date2019-01-24
Date Reported to FDA2019-01-24
Date Reported to Mfgr2019-01-25
Date Added to Maude2019-01-25
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOLOX DELTA CERAMIC HEADS 36MM
Generic NamePROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER
Product CodeMAY
Date Received2019-01-25
Model Number12-115121
Catalog Number12-115121
Lot Number2968724
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBIOMET, INC.
Manufacturer Address56 EAST BELL DR. P.O. BOX 587 WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-25

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