FDA Adverse Event Injury Summary report: N

3.5 LCP SUP CLAV PL LAT EXTN/7H/LT/120

MDR report key: 12388118 · Received August 30, 2021

Report

Report Number
2939274-2021-05009
Event Type
Injury
Date Received
August 30, 2021
Report Date
August 24, 2021
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
HRS
UDI-DI
10886982033277
PMA / PMN Number
K073186
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. 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, THE PATIENT UNDERWENT A FRACTURE FIXATION FOR A SHAFT FRACTURE UTILIZING LCP SUPERIOR CLAVICLE PLATE. DBM 5CC WAS USED AS AN ADDITIONAL SURGICAL INTERVENTION. A REOPERATION WAS DONE DUE TO HARDWARE REMOVAL, PATIENT COULD FEEL IMPLANT. UNION WAS ACHIEVED AFTER 8 WEEKS. NO POST-OPERATIVE COMPLICATIONS REPORTED. CONCOMITANT DEVICES REPORTED: UNK, SCREWS: (PART# UNKNOWN; LOT# UNKNOWN; QUANTITY: 4). THIS REPORT IS FOR (1) 3.5 LCP SUP CLAV PL LAT EXTN/7H/LT/120. THIS IS REPORT 1 OF 5 FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1285881 3.5 LCP SUP CLAV PL LAT EXTN/7H/LT/120 PLATE, FIXATION, BONE HRS WRIGHTS LANE SYNTHES USA PRODUCTS LLC 02.112.093 10886982033277

Patients

Seq Age Sex Outcome Treatment
1 43 YR Required Intervention