FDA Adverse Event Malfunction Summary report: N

CUP OSTEOTOME 56MM X 120 DEG

MDR report key: 11495681 · Received March 16, 2021

Report

Report Number
1818910-2021-05177
Event Type
Malfunction
Date Received
March 16, 2021
Date of Event
March 1, 2021
Report Date
February 28, 2021
Manufacturer
DEPUY ORTHOPAEDICS INC US
Product Code
HWM
UDI-DI
10603295123101
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NZ
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # (B)(4). INVESTIGATION SUMMARY: EXAMINATION OF THE RETURNED INSTRUMENT CONFIRMED THE COMPLAINT. DEPUY-SYNTHES CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED, AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY. DEVICE HISTORY LOT: THE PRODUCT INVESTIGATION FOUND NO EVIDENCE SUSPECTING AN ERROR IN THE MANUFACTURING OR MATERIAL THAT WOULD BE A CONTRIBUTING FACTOR IN THE REPORTED ALLEGATION(S). A MANUFACTURING RECORDS EVALUATION (MRE) WAS NOT PERFORMED.

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

IN REMOVING AN ACETABULAR SHELL FOR SCHEDULED REVISION, SURGEON BROKE TWO (2) CURVED OSTEOTOMES FROM OUR LOAN MORELANDS CEMENTLESS REMOVAL INSTRUMENTS KIT. IN EACH INSTANCE, THE TIP OF THE OSTEOTOME SNAPPED, LIKELY DUE TO BEING USED AS A LEVER BEHIND THE ACETABULAR SHELL. PRODUCT CODES D242212000 & D2422-13. METAL FRAGMENT WAS A SINGLE PIECE ON EACH OCCASION AND WAS EASILY RETRIEVED FROM THE PATIENT WITH NO PATIENT HARM OR IMPACT ON SURGICAL TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
394441 CUP OSTEOTOME 56MM X 120 DEG HIP INSTRUMENTS : CUTTING INSTRUMENTS HWM DEPUY ORTHOPAEDICS INC US 2422-13-000 AK0396B 10603295123101

Patients

Seq Age Sex Outcome Treatment
1