MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-10-05 for TC TENOTOMY SCISSDELCVD1/SERR130MM DO250R manufactured by Aesculap Ag.
[89697682]
(b)(4). Manufacturing site evaluation: evaluation on-going
Patient Sequence No: 1, Text Type: N, H10
[89697684]
Country of complaint: usa. Tips of tenotomy scissor broke off & hinge broke. Scissor broke while surgeon was using it. It ended up in 4 pieces. X-ray was negative, all pieces are accounted for. Type of surgery unknown at this time, enquiry has been made. No patient harm reported. No surgical delay reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610612-2017-00492 |
| MDR Report Key | 6917885 |
| Date Received | 2017-10-05 |
| Date of Report | 2018-03-06 |
| Date of Event | 2017-08-18 |
| Date Facility Aware | 2017-09-29 |
| Date Mfgr Received | 2017-09-18 |
| Date Added to Maude | 2017-10-05 |
| 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 | MS. NICOLE BROYLES |
| Manufacturer Street | 615 LAMBERT POINTE DRIVE |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| Manufacturer Phone | 3145515988 |
| Manufacturer G1 | AESCULAP AG |
| Manufacturer Street | PO BOX 40 |
| Manufacturer City | TUTTLINGEN, 78501 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 78501 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | TC TENOTOMY SCISSDELCVD1/SERR130MM |
| Generic Name | DENTAL SCISSORS |
| Product Code | EGN |
| Date Received | 2017-10-05 |
| Returned To Mfg | 2017-09-28 |
| Model Number | DO250R |
| Catalog Number | DO250R |
| Lot Number | 1208530B |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AESCULAP AG |
| Manufacturer Address | PO BOX 40 TUTTLINGEN, 78501 GM 78501 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2017-10-05 |