ORTHOLOC(TM) SCREW
Report
- Report Number
- 1043534-2014-00127
- Event Type
- Malfunction
- Date Received
- May 12, 2014
- Date of Event
- April 2, 2014
- Report Date
- April 2, 2014
- Manufacturer
- WRIGHT MEDICAL TECHNOLOGY, INC.
- Product Code
- HWC
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- OTHER
Narratives
VISUAL INSPECTION FOUND THAT THE SCREW DOES HAVE THREAD PEELING FROM THE SCREW. ANALYSIS OF THE RETURNED PRODUCT FOUND THE SCREW TO BE WITHIN SPECIFICATION. ANALYSIS OF THE RETURNED PRODUCT INDICATES THAT THE SCREW COULD HAVE BEEN A CONTRIBUTOR TO THE REPORTED EVENT. THE SCREW HAS PEELING THREAD INDICATING THAT IT MAY HAVE BEEN INSERTED THROUGH THE PLATE AT AN ANGLE CAUSING THE THREAD TO PEEL. BASED ON ANALYSIS, A DEFINITIVE ROOT CAUSE COULD NOT BE DETERMINED. HOWEVER THE MOST LIKELY ROOT CAUSE WAS USER TECHNIQUE.
THIS IS A REPORTABLE MALFUNCTION. INVESTIGATION IS NOT COMPLETE. TRENDS WILL BE EVALUATED. THIS REPORT WILL BE UPDATED WHEN THE INVESTIGATION IS COMPLETE. THIS IS THE SAME EVENT AS 1043534-2014-00128.
ALLEGEDLY THREADS "PEELING" OFF SEVERAL SCREWS (LOCK AND NON LOCK) WHILE INSERTED INTO RIGHT MEDIUM LATERAL FIBULA PLAGE. THE IMPLANTATION SITE WAS THE LATERAL FIBULA FRACTURE AND THE ISSUE WAS RESOLVED BY SWAPPED SCREWS. THE SALES REP WAS PRESENT AT THE PROCEDURE; SURGERY WAS NOT EXTENDED MORE THAN 30 MINS; INCIDENT OCCURRED DURING SURGERY. EMAILED SALES REP (B)(4) ON (B)(4) 2014 FOR PRODUCT INFORMATION, TRACKING NUMBER FOR PRODUCTS BEING SENT BACK AND IF SHE HAD ANY KNOWLEDGE ON THE HOSPITAL FILING A MDR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 284335 | ORTHOLOC(TM) SCREW | SMALL JOINT COMPONENT | HWC | WRIGHT MEDICAL TECHNOLOGY, INC. | 1363566 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |