FDA Adverse Event Malfunction Summary report: N

UNK - SCREWS: LOCKING

MDR report key: 12805220 · Received November 12, 2021

Report

Report Number
2939274-2021-06675
Event Type
Malfunction
Date Received
November 12, 2021
Report Date
October 19, 2021
Manufacturer
WRIGHTS LANE SYNTHES USA PRODUCTS LLC
Product Code
HWC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # (B)(4). THIS REPORT IS FOR AN UNK - SCREWS: LOCKING/UNKNOWN LOT. PART AND LOT NUMBERS ARE UNKNOWN; UDI NUMBER IS UNKNOWN. 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 AS NO PRODUCT WAS RECEIVED. THE INVESTIGATION COULD NOT BE COMPLETED, NO PRODUCT WAS RECEIVED; NO CONCLUSION COULD BE DRAWN AT THE TIME OF FILING THIS REPORT. BASED ON THE INFORMATION AVAILABLE, NO FURTHER ACTION IS REQUIRED AT THIS TIME. COMPLAINT INFORMATION IS TRENDED ON A REGULAR BASIS TO DETERMINE IF FURTHER INVESTIGATION IS WARRANTED. 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 · 0

IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT UNDERWENT FOR A REVISION SURGERY DUE TO SCREW PROMINENCE AND POTENTIAL LOSS OF FIXATION ON (B)(6) 2021. DISTAL MOST LOCKING SCREW IN AN RFN ADVANCED BACKED OUT 2 MONTHS AFTER INSERTION. IT WAS UNKNOWN IF THE REVISION SURGERY COMPLETED SUCCESSFULLY. THE PATIENT'S STATUS IS UNKNOWN. CONCOMITANT DEVICE REPORTED: UNK - NAILS: RAFN (PART # UNKNOWN; LOT # UNKNOWN; QUANTITY: 1), UNK - SCREWS: NAIL DISTAL LOCKING (PART # UNKNOWN; LOT # UNKNOWN; QUANTITY: UNKNOWN), UNK - END CAP (PART # UNKNOWN; LOT# UNKNOWN; QUANTITY: 1). THIS COMPLAINT INVOLVES ONE(1) DEVICE. THIS REPORT IS FOR ONE (1) UNK - SCREWS: LOCKING. THIS IS REPORT 1 OF 1 FOR (B)(4). RELATED PRODUCT COMPLAINT: (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1705552 UNK - SCREWS: LOCKING SCREW, FIXATION, BONE HWC WRIGHTS LANE SYNTHES USA PRODUCTS LLC

Patients

Seq Age Sex Outcome Treatment
1 Unknown UNK - END CAPS: RAFN| UNK - NAILS: RAFN| UNK - SCREWS: NAIL DISTAL LOCKING