FDA Adverse Event
Malfunction
Summary report: N
MSP METATARSAL SHORTENING SYSTEM
MDR report key: 10313829
·
Received July 23, 2020
Report
- Report Number
- 3009540749-2020-00017
- Event Type
- Malfunction
- Date Received
- July 23, 2020
- Date of Event
- February 22, 2020
- Report Date
- July 23, 2020
- Manufacturer
- NEXTREMITY SOLUTIONS
- Product Code
- HRS
- PMA / PMN Number
- K140724
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- 003
Narratives
Additional Manufacturer Narrative · 1
CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED BECAUSE IT REMAINS IMPLANTED. DEVICE HISTORY RECORDS RELATED TO THE EVENT WERE REVIEWED. THERE WERE NO NON-CONFORMANCES DETECTED THROUGH THE DEVICE HISTORY RECORD REVIEW. IF ADDITIONAL INFORMATION IS OBTAINED WHICH CHANGES THE OUTCOME OF THE INVESTIGATION, A FOLLOW-UP REPORT WILL BE FILED.
Description of Event or Problem · 1
IT WAS REPORTED A METATARSAL SHORTENING SYSTEM PROCEDURE WAS PERFORMED ON (B)(6) 2020. ON (B)(6) 2020 SURGEON REPORTED THE MSP PLATE CRACKED FROM THE SLIT PORTION TO THE DYNAMIC HOLE. THE PATIENT HAS NO PAIN AND THE PRODUCT REMAINS IMPLANTED. SURGEON IS MONITORING THE PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 779565 | MSP METATARSAL SHORTENING SYSTEM | PLATE | HRS | NEXTREMITY SOLUTIONS | 168415217B |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |