ZIMMER, INC. ZIMMER PRE ALLOCATED 736196 KNEE IMPLANT; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL
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Model Number 5988-04 |
Device Problems
Mechanical Problem (1384); Noise, Audible (3273)
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Patient Problems
Failure of Implant (1924); Pain (1994); Swelling (2091)
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Event Date 06/01/2020 |
Event Type
Injury
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Event Description
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I've had swelling on and off since device was put in 4 and a half years ago; 2 months ago i started to feel pain, pinching, popping and locking up.I have an appointment scheduled with a knee specialist (b)(6).Fda safety report id# (b)(4).
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Search Alerts/Recalls
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