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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ZIMMER BIOMET, INC. PERSONA PARTIAL KNEE CEMENTED FEMORAL COMPONENT SIZE 5 RIGHT MEDIAL; PROSTHESIS, KNEE

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ZIMMER BIOMET, INC. PERSONA PARTIAL KNEE CEMENTED FEMORAL COMPONENT SIZE 5 RIGHT MEDIAL; PROSTHESIS, KNEE Back to Search Results
Model Number N/A
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Pain (1994); Numbness (2415)
Event Date 12/12/2019
Event Type  Injury  
Manufacturer Narrative
(b)(4).Report source: foreign: (b)(4).No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Review of the device history records identified no deviations or anomalies during manufacturing related to the reported event.The reported products were reviewed for compatibility with no issues noted.Review of complaint history identified additional similar complaints for the reported items and no additional similar complaints for the reported part and lot combinations.Complaints are monitored through monthly complaint review (reference (b)(4)) in order to identify potential adverse trends.Medical records/radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: onset findings: pt seen in clinic reporting significant discomfort to medial aspect of r knee.Ct scan showed increased activity under tibial plate and remodeling from clear evidence of overload.Patient seen in clinic approximately 8 months from previous visit reporting continued medial pain and numbness to lateral side of study knee.X-rays show no significant changes.Pt advised to continue with weight reduction.Currently at (b)(6).The complaint cannot be confirmed.A definitive root cause cannot be determined.No corrective actions, preventive actions, or field actions resulted after investigation of this event.Additional associated products and mdrs: 42538000602 persona partial knee cemented tibial component size f right lot# 63886720 mdr: 0001825034-2020-04346.42528200609 persona partial articular surface right medial size f 9mm lot# 63449781 mdr: 0001825034-2020-03456.
 
Event Description
It is reported that a patient experienced significant discomfort and numbness in the medial aspect of the knee nineteen (19) months following right knee arthroplasty.A the patient was advised to continue reducing weight and no medical intervention was performed.Attempts have been made for additional information, however, no additional information is available at this time.
 
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Brand Name
PERSONA PARTIAL KNEE CEMENTED FEMORAL COMPONENT SIZE 5 RIGHT MEDIAL
Type of Device
PROSTHESIS, KNEE
Manufacturer (Section D)
ZIMMER BIOMET, INC.
56 e. bell drive
warsaw IN 46582
Manufacturer (Section G)
ZIMMER BIOMET, INC.
56 e. bell drive
warsaw IN 46582
Manufacturer Contact
christina arnt
56 e. bell dr.
warsaw, IN 46582
5745273773
MDR Report Key10987604
MDR Text Key220890142
Report Number0001825034-2020-04345
Device Sequence Number1
Product Code HSX
UDI-Device Identifier00880304808560
UDI-Public(01)00880304808560
Combination Product (y/n)N
Reporter Country CodeUK
PMA/PMN Number
K161592
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Reporter Occupation Physician
Type of Report Initial
Report Date 12/10/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/10/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model NumberN/A
Device Catalogue Number42558000502
Device Lot Number63856205
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Date Manufacturer Received12/03/2020
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured12/19/2018
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Removal/Correction NumberN/A
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Weight151
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