FDA Adverse Event Malfunction Summary report: N

SROM TRI MILL CUTTER BLUE 20

MDR report key: 16277819 · Received February 1, 2023

Report

Report Number
1818910-2023-02604
Event Type
Malfunction
Date Received
February 1, 2023
Date of Event
January 19, 2023
Report Date
February 1, 2023
Manufacturer
DEPUY ORTHOPAEDICS INC US
Product Code
HTZ
UDI-DI
10603295145486
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). DEPUY SYNTHES IS SUBMITTING THIS REPORT PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH DEPUY SYNTHES HAS NOT BEEN ABLE TO INVESTIGATE OR VERIFY PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY FDA, DEPUY SYNTHES OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE DEVICE, DEPUY SYNTHES, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. 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 WAS RECEIVED FOR EXAMINATION, THEREFORE THE REPORTED EVENT COULD NOT BE CONFIRMED. 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 (MRE), WAS NOT POSSIBLE BECAUSE THE REQUIRED LOT CODE WAS NOT PROVIDED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE SCRUB TECH NOTICED THE IMPACTOR HANDLE WAS STRIPPED AND THAT THE COLOR BAND FELL OFF THE REAMER. INSTRUMENTS WERE NOT USED. THERE WAS NO SURGICAL DELAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1348104 SROM TRI MILL CUTTER BLUE 20 HIP INSTRUMENTS : REAMERS HTZ DEPUY ORTHOPAEDICS INC US 2576-04-020 10603295145486

Patients

Seq Age Sex Outcome Treatment
1 Female