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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. JII XR ART ISRT LAT SZ 5-6 LT 9MM -2 DEG; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRND, CMNTD, PLYMR/METAL/PLYMR
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SMITH & NEPHEW, INC. JII XR ART ISRT LAT SZ 5-6 LT 9MM -2 DEG; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRND, CMNTD, PLYMR/METAL/PLYMR Back to Search Results
Model Number 74024025
Medical Device Problem Code Mechanical Problem (1384)
Health Effect - Clinical Code Loss of Range of Motion (2032)
Date of Event 01/10/2019
Type of Reportable Event Serious Injury
Event or Problem Description
It was reported that after primary surgery, using journey ii xr implants patient had knee stiffness and decreased range of motion.Despite physical therapy; adequate pain management, the patient was unable to maintain an acceptable post operative knee range of motion.A manipulation under anesthesia was performed to resolve the event.Patient gained significant range of motion and was able to achieve more terminal flexion.
 
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Brand Name
JII XR ART ISRT LAT SZ 5-6 LT 9MM -2 DEG
Common Device Name
PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRND, CMNTD, PLYMR/METAL/PLYMR
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
MDR Report Key9957529
Report Number1020279-2020-01298
Device Sequence Number2808734
Product Code JWH
UDI-Device Identifier00885556616536
UDI-Public00885556616536
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K152726
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2018
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 12/04/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Expiration Date09/17/2026
Device Model Number74024025
Device Catalogue Number74024025
Device Lot Number16JM08911
Initial Date Received by Manufacturer 03/23/2020
Supplement Date Received by Manufacturer12/02/2020
Initial Report FDA Received Date04/14/2020
Supplement Report FDA Received Date12/05/2020
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
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