FDA Adverse Event Malfunction Summary report: N

2.5MM DRILL BIT/QC/GOLD/110MM

MDR report key: 12432118 · Received September 7, 2021

Report

Report Number
2939274-2021-05202
Event Type
Malfunction
Date Received
September 7, 2021
Date of Event
August 9, 2021
Report Date
August 9, 2021
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
GFA
UDI-DI
10886982186317
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL PRODUCT CODE: HWE, HSZ, GFF. COMPLAINANT PART IS EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION BUT HAS YET TO BE RECEIVED. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. PRODUCT WAS NOT RETURNED. BASED ON THE INFORMATION AVAILABLE, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. THIS COMPLAINT WILL BE ACCOUNTED FOR AND MONITORED VIA POST MARKET SURVEILLANCE ACTIVITIES. IF ADDITIONAL INFORMATION IS MADE AVAILABLE, THE INVESTIGATION WILL BE UPDATED AS APPLICABLE. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. 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

IT WAS REPORTED THAT ON (B)(6) 2021 DURING THE PROCEDURE THE 2.5MM DRILL BITS WAS BROKEN. PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. THIS REPORT IS FOR ONE (1) 2.5MM DRILL BIT/QC/GOLD/110MM. THIS IS REPORT 2 OF 2 FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1330929 2.5MM DRILL BIT/QC/GOLD/110MM BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL GFA WRIGHTS LANE SYNTHES USA PRODUCTS LLC 310.25 10886982186317

Patients

Seq Age Sex Outcome Treatment
1 42 YR 2.5MM DRILL BIT/QC/GOLD/110MM