Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )
Report
- Report Number
- 0001526350-2023-00993
- Event Type
- Malfunction
- Date Received
- August 28, 2023
- Report Date
- August 28, 2023
- Manufacturer
- ZIMMER SURGICAL, INC.
- Product Code
- FZW
- PMA / PMN Number
- PREAMENDMENT
- Removal / Correction Number
- N/A
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
THIS EVENT HAS BEEN RECORDED BY ZIMMER BIOMET UNDER (B)(4). G2 FOREIGN: CANADA. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORT: 0001526350-2023-00214-2. THE INVESTIGATION IS COMPLETE. THIS IS AN INITIAL FINAL REPORT SUBMISSION. REVIEW OF THE MOST RECENT REPAIR RECORD IDENTIFIED THE FOLLOWING RELATED REPAIR: THE CUTTER FAILED TESTING DUE TO AN INCOMPLETE CUT. THE CUTTER WILL NEED REPLACEMENT. REVIEW OF THE DEVICE HISTORY RECORD IDENTIFIED NO DEVIATIONS OR ANOMALIES DURING MANUFACTURING RELATED TO THE REPORTED EVENT. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED. THE EVENT IS CONFIRMED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.
IT WAS REPORTED THAT THE DEVICE WAS NOT MESHING. THERE WAS NO HARM OR DELAY REPORTED. DUE DILIGENCE IS COMPLETE. NO ADVERSE EVENTS WERE REPORTED AS A RESULT OF THIS MALFUNCTION. AT PRODUCT EVALUATION INVESTIGATION THE CUTTER FAILED TESTING DUE TO AN INCOMPLETE CUT. NO ADDITIONAL EVENT INFORMATION AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1338970 | Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP ) | EXPANDER, SURGICAL, SKIN GRAFT | FZW | ZIMMER SURGICAL, INC. | N/A | 60227532 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Prefer Not To Disclose |