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 2019-04-03 for SMALL WIRE CUTTER 160MM 391.900 manufactured by Oberdorf Synthes Produktions Gmbh.
[140894700]
Device used in a veterinary case - no patient information will be reported. The investigation could not be completed; no conclusion could be drawn, as no product was received. Based on the information available, it has been determined that no corrective and/or preventative action is proposed. This complaint will be accounted for and monitored via post market surveillance activities. If additional information is made available, the investigation will be updated as applicable. Device was used for treatment, not diagnosis. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Patient Sequence No: 1, Text Type: N, H10
[140894701]
Device report from synthes reports an event in (b)(6) as follows: veterinary complaint: it was reported that on (b)(6) 2019, the pair of pin cutters were used about three (3) times where the edge was noted to separate. The issue was found during inspection. There was no patient or procedure involvement. This report is for one (1) small wire cutter 160mm. This is report 1 of 1 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8030965-2019-62460 |
| MDR Report Key | 8478730 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-04-03 |
| Date of Report | 2019-03-08 |
| Date of Event | 2019-03-08 |
| Date Mfgr Received | 2019-06-04 |
| Device Manufacturer Date | 2018-04-26 |
| Date Added to Maude | 2019-04-03 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | KARA DITTY-BOVARD |
| Manufacturer Street | 1302 WRIGHTS LANE EAST |
| Manufacturer City | WEST CHESTER PA 19380 |
| Manufacturer Country | US |
| Manufacturer Postal | 19380 |
| Manufacturer Phone | 6103142063 |
| 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 | SMALL WIRE CUTTER 160MM |
| Generic Name | CUTTER,WIRE |
| Product Code | HXZ |
| Date Received | 2019-04-03 |
| Returned To Mfg | 2019-06-04 |
| Catalog Number | 391.900 |
| Lot Number | T157474 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Manufacturer Address | EIMATTSTRASSE 3 OBERDORF 4436 SZ 4436 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-04-03 |