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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ZIMMER BIOMET, INC. ULNAR COMPONENT PLASMA SPRAYED SIZE 5 75 MM LENGTH RIGHT ELBOW, PROSTHESIS

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ZIMMER BIOMET, INC. ULNAR COMPONENT PLASMA SPRAYED SIZE 5 75 MM LENGTH RIGHT ELBOW, PROSTHESIS Back to Search Results
Catalog Number 00840002507
Device Problem Loosening of Implant Not Related to Bone-Ingrowth (4002)
Patient Problem Failure of Implant (1924)
Event Date 02/15/2021
Event Type  Injury  
Manufacturer Narrative
(b)(4). Report source: foreign: (b)(6). Concomitant medical products: humeral screw kit 2 humeral screws, cat: 00840009000, lot: 62908109. Humeral component plasma sprayed size 4 150 mm, cat: 00840004415, lot: 63399782. Customer has indicated that the product will not be returned to zimmer biomet for investigation. The investigation is in process. Once the investigation has been completed, a follow-up report will be submitted.
 
Event Description
It was reported that the patient was noted to have ulnar and humeral component loosening in a radio graph review. A revision procedure has not been indicated at this time.
 
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Brand NameULNAR COMPONENT PLASMA SPRAYED SIZE 5 75 MM LENGTH RIGHT
Type of DeviceELBOW, PROSTHESIS
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 Key12693438
MDR Text Key278358362
Report Number0001822565-2021-03106
Device Sequence Number1
Product Code JDC
Combination Product (y/n)N
Reporter Country CodeUK
PMA/PMN Number
K123862
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Reporter Occupation
Type of Report Initial
Report Date 10/25/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/25/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator
Device Catalogue Number00840002507
Device Lot Number63399782
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Event Location No Information
Date Manufacturer Received09/27/2021
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured07/29/2016
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient Treatment Data
Date Received: 10/25/2021 Patient Sequence Number: 1
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