FDA Adverse Event Malfunction Summary report: N

SMARTSET HV BONE CEMENT 40G

MDR report key: 14218085 · Received April 27, 2022

Report

Report Number
1818910-2022-07628
Event Type
Malfunction
Date Received
April 27, 2022
Date of Event
April 15, 2022
Report Date
April 27, 2022
Manufacturer
DEPUY ORTHOPAEDICS INC US
Product Code
LOD
UDI-DI
10603295168331
PMA / PMN Number
K033563
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # (B)(4). IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT (B)(4). INVESTIGATION SUMMARY: NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. THE INFORMATION RECEIVED WILL BE RETAINED FOR POTENTIAL SERIES INVESTIGATIONS IF TRIGGERED BY TREND ANALYSIS, POST MARKET SURVEILLANCE, OR OTHER EVENTS WITHIN THE QUALITY SYSTEM. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY. DEVICE HISTORY LOT: A MANUFACTURING RECORD EVALUATION (NC SEARCH) WAS PERFORMED FOR THE FINISHED DEVICE PRODUCT CODE 3092040, LOT NUMBER 9859816, AND NO NON-CONFORMANCES / MANUFACTURING IRREGULARITIES WERE IDENTIFIED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE CEMENT DID NOT SET UP PROPERLY. WAS NOT SET UP UNTIL 20 MINUTES AFTER INITIAL MIX. SURGICAL TECH REFUSED TO FOLLOW PROPER MIXING TECHNIQUE AS DIRECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1792636 SMARTSET HV BONE CEMENT 40G BONE CEMENT : BONE CEMENT LOD DEPUY ORTHOPAEDICS INC US 3092-040 9859816 10603295168331

Patients

Seq Age Sex Outcome Treatment
1 Male