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TRABECULAR METAL ACETABULAR AUGMENT Adverse Event — Injury (MDR 3005751028-2020-00052)

TRABECULAR METAL ACETABULAR AUGMENT Adverse Event — Injury (MDR 3005751028-2020-00052) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRABECULAR METAL ACETABULAR AUGMENT; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER TMT.

DeviceTRABECULAR METAL ACETABULAR AUGMENT
Generic namePROSTHESIS, HIP
ManufacturerZIMMER TMT
Report number3005751028-2020-00052
Event typeInjury
Product problemY
Date received2020-04-28
Report sourceFOREIGN, LITERATURE
Narrative(B)(4). CONCOMITANT MEDICAL PRODUCT: UNKNOWN ACETABULAR SHELL; UNKNOWN FEMORAL STEM; UNKNOWN FEMORAL HEAD; UNKNOWN ACETABULAR LINER. REPORT SOURCE: (B)(6). O'NEILL, C. J., CREEDON, S. B., BRENNAN, S. A., O'MAHONY, F. J., LYNHAM, R. S., GUERIN, S., . . . HARTY, J. A. (2018). ACETABULAR REVISION USING TRABECULAR METAL AUGMENTS FOR PAPROSKY TYPE 3 DEFECTS. RESULTS OF TOTAL HIP ARTHROPLASTY AFTER CORE
SourceopenFDA MAUDE (device adverse events)

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