MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-11-16 for CHISEL BLADE 16MM 399.560 manufactured by Wrights Lane Synthes Usa Products Llc.
[128070295]
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. This report is a duplicate report for manufacturer report number 2939274-2018-54832. At this time we have not received successful passed acknowledgments for that report number so this report is being submitted to ensure successful receipt of the information. Since the initial submission of the report, the part has come back and this medwatch report has been update accordingly to reflect that information. The device was received, the investigation could not be completed, and no conclusion could be drawn, as product is entering the complaint system. A review of the device history records has been requested. Device was used for treatment, not diagnosis.
Patient Sequence No: 1, Text Type: N, H10
[128070296]
Device report from synthes reports an event in (b)(6) as follows: it was reported that on an unknown date, the chisel blades were found in medical device reprocessing department (mdrd) and tagged as broken. There were no patient and procedure involvement. This complaint involves ten (10) devices. This report is 6 of 10 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2939274-2018-55012 |
| MDR Report Key | 8081070 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2018-11-16 |
| Date of Report | 2018-10-18 |
| Date Mfgr Received | 2019-01-09 |
| Device Manufacturer Date | 2016-08-24 |
| Date Added to Maude | 2018-11-16 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MICHAEL COTE |
| Manufacturer Street | 1302 WRIGHT LANE EAST |
| Manufacturer City | WEST CHESTER PA 19380 |
| Manufacturer Country | US |
| Manufacturer Postal | 19380 |
| Manufacturer Phone | 6107195000 |
| Manufacturer G1 | SYNTHES TUTTLINGEN |
| Manufacturer Street | UNTER HASSLEN 5 |
| Manufacturer City | TUTTLINGEN 78532 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 78532 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CHISEL BLADE 16MM |
| Generic Name | CHISEL,SURGICAL INSTRUMENT |
| Product Code | FZO |
| Date Received | 2018-11-16 |
| Returned To Mfg | 2018-11-08 |
| Catalog Number | 399.560 |
| Lot Number | T140618 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | WRIGHTS LANE SYNTHES USA PRODUCTS LLC |
| Manufacturer Address | 1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 US 19380 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-11-16 |