FDA Adverse Event Injury Summary report: N

3.5MM LCP SUP ANT CLAVICLE PL W/LAT EXTN 5H/LT/94MM

MDR report key: 12506679 · Received September 21, 2021

Report

Report Number
2939274-2021-05647
Event Type
Injury
Date Received
September 21, 2021
Report Date
July 23, 2021
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
HRS
UDI-DI
10886982032690
PMA / PMN Number
K111540
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 ON AN UNKNOWN DATE, THE PATIENT UNDERWENT A SHAFT FRACTURE FIXATION UTILIZING LOCKING COMPRESSION PLATE (LCP) SUPERIOR-ANTERIOR CLAVICLE PLATE. UNION WAS ACHIEVED AFTER 12 WEEKS. HARDWARE REMOVAL WAS DONE DUE TO PROMINENT HARDWARE. PATIENT OUTCOME IS UNKNOWN. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR ONE (1) 3.5MM LCP SUP ANT CLAVICLE PL W/LAT EXTN 5H/LT/94MM. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1407800 3.5MM LCP SUP ANT CLAVICLE PL W/LAT EXTN 5H/LT/94MM PLATE, FIXATION, BONE HRS WRIGHTS LANE SYNTHES USA PRODUCTS LLC 02.112.013 10886982032690

Patients

Seq Age Sex Outcome Treatment
1 20 YR Required Intervention UNKNOWN-SCREWS