23MM MOD REV HIP BDY/BLT +10MMCOMPONENT LEVEL 9006-1-123 Adverse Event — Injury (MDR 0002249697-2020-00803)

Name: 23MM MOD REV HIP BDY/BLT +10MMCOMPONENT LEVEL 9006-1-123 Adverse Event — Injury (MDR 0002249697-2020-00803)
Creator: DeviceEvents

23MM MOD REV HIP BDY/BLT +10MMCOMPONENT LEVEL 9006-1-123 Adverse Event — Injury (MDR 0002249697-2020-00803) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 23MM MOD REV HIP BDY/BLT +10MMCOMPONENT LEVEL 9006-1-123; Generic name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, P

Device	23MM MOD REV HIP BDY/BLT +10MMCOMPONENT LEVEL 9006-1-123
Generic name	PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNC
Manufacturer	STRYKER ORTHOPAEDICS-MAHWAH
Report number	0002249697-2020-00803
Event type	Injury
Product problem	N
Date received	2020-04-27
Report source	COMPANY REPRESENTATIVE
Narrative	PATIENT WAS TAKEN BACK FOR INSTABILITY. UNSURE FROM THE INFORMATION AT THE HOSPITAL WHAT WAS TAKEN OUT. THERE IS NO MORE INFORMATION TO INFORM.
Source	openFDA MAUDE (device adverse events)

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