GPS DUAL TIP MALABLE 20GAX4IN
Report
- Report Number
- 0001825034-2017-03617
- Event Type
- Malfunction
- Date Received
- June 5, 2017
- Date of Event
- May 9, 2017
- Report Date
- November 10, 2017
- Manufacturer
- BIOMET ORTHOPEDICS
- Product Code
- KYZ
- PMA / PMN Number
- PK940371
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
Narratives
REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTIONS ARE REQUIRED. THE ROOT CAUSE OF THE REPORTED EVENT WAS DETERMINED TO BE A LABELING DEFICIENCY AT THE SUPPLIER. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.
THIS FOLLOW-UP REPORT IS BEING FILED TO RELAY ADDITIONAL INFORMATION, WHICH WAS UNKNOWN AT THE TIME OF THE INITIAL MEDWATCH.
(B)(6). DEVICE PRODUCT CODE - KYZ. CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.
IT WAS REPORTED THAT THE EXPIRATION DATES ON THE IMPLANT STICKERS AND OUTER PACKAGING DID NOT MATCH. THE IMPLANT STICKERS HAD ON THE INCORRECT EXPIRATION DATE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 394323 | GPS DUAL TIP MALABLE 20GAX4IN | SYRINGE, IRRIGATING (NON DENTAL) | KYZ | BIOMET ORTHOPEDICS | 170250 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR |