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