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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ZIMMER SWITZERLAND MANUFACTURING GMBH PROXIMAL HUMERUS, LEFT, LONG, 8.5X220MM AFFIXUS NATURAL NAIL SYSTEM HUMERAL NAIL
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ZIMMER SWITZERLAND MANUFACTURING GMBH PROXIMAL HUMERUS, LEFT, LONG, 8.5X220MM AFFIXUS NATURAL NAIL SYSTEM HUMERAL NAIL Back to Search Results
Model Number N/A
Device Problem Use of Device Problem (1670)
Patient Problem Insufficient Information (4580)
Event Date 01/21/2022
Event Type  Injury  
Event Description
It was reported that operation was performed with ann nail system. After 2 months from the initial, surgeon found a screw of the proximal screws was backed out from the proper position. The surgeon keep an eye on the patient condition as well as no revision will be planned so far.
 
Manufacturer Narrative
Concomitant medical products: ann cort bone screw 4 x 26mm; catalog#: 47-2486-126-40; lot#: 3054512. Ann cort bone screw 4 x 28mm; catalog#: 47-2486-128-40; lot#: 3054458. Affixus ph nl cap 0mm; catalog#: 47-2488-010-00; lot#: 3076770. The manufacturer did not receive x-rays, or other source documents for review. The manufacturer did not receive the device for investigation. The lot number of the device was received. The device history records will be reviewed during investigation. A cause for this specific event cannot be ascertained from the information provided. As soon as supplemental information becomes available an updated report will be submitted. Zimmer biomet¿s reference number of this file is (b)(4). The following reports are associated with this event: 0009613350-2022-00104; 0009613350-2022-00105; 0009613350-2022-00106; 0009613350-2022-00107.
 
Manufacturer Narrative
Concomitant medical products: ann cort bone screw 4 x 26mm; catalog#: 47-2486-126-40; lot#: 3054512. Ann cort bone screw 4 x 28mm; catalog#: 47-2486-128-40; lot#: 3054458. Affixus ph nl cap 0mm; catalog#: 47-2488-010-00; lot#: 3076770. The manufacturer did not receive x-rays, or other source documents for review. The manufacturer did not receive the device for investigation. The lot number of the device was received. The device history records will be reviewed during investigation. A cause for this specific event cannot be ascertained from the information provided. As soon as supplemental information becomes available an updated report will be submitted. Zimmer biomet¿s reference number of this file is (b)(4). The following reports are associated with this event: 0009613350-2022-00104; 0009613350-2022-00105; 0009613350-2022-00106; 0009613350-2022-00107.
 
Event Description
It was reported that operation was performed with ann nail system. After 2 months from the initial, surgeon found a screw of the proximal screws was backed out from the proper position. The surgeon keep an eye on the patient condition as well as no revision will be planned so far.
 
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Brand NamePROXIMAL HUMERUS, LEFT, LONG, 8.5X220MM
Type of DeviceAFFIXUS NATURAL NAIL SYSTEM HUMERAL NAIL
Manufacturer (Section D)
ZIMMER SWITZERLAND MANUFACTURING GMBH
sulzer allee 8
sulzer industrie park
winterthur 8404
SZ 8404
Manufacturer (Section G)
ZIMMER SWITZERLAND MANUFACTURING GMBH
sulzer allee 8
sulzer industrie park
winterthur 8404
SZ 8404
Manufacturer Contact
christina arnt
56 e. bell dr.
warsaw, IN 46582
5745273773
MDR Report Key13583791
MDR Text Key285988301
Report Number0009613350-2022-00108
Device Sequence Number1
Product Code HSB
Combination Product (y/n)N
Reporter Country CodeJA
PMA/PMN Number
K181827
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional
Reporter Occupation
Type of Report Initial,Followup
Report Date 04/12/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/23/2022
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator
Device Model NumberN/A
Device Catalogue Number47-2496-221-08
Device Lot Number3026730
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Date Manufacturer Received03/18/2022
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured05/20/2020
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 Treatment Data
Date Received: 02/23/2022 Patient Sequence Number: 1
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