MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-08-16 for KOCHER-OCHSNER FORCEPS STR 1X2 225MM BH648R manufactured by Aesculap Ag.
[117385372]
Investigation: no product is at hand. Conclusion and root cause: the failure is most probably handling related. Rational: we did not receive the complaint product. Based on our experience, we assume that an overload situation led to the breakage. No capa is necessary.
Patient Sequence No: 1, Text Type: N, H10
[117385373]
Country of complaint: usa. Io tip of forcep is broken.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610612-2018-00328 |
| MDR Report Key | 7790279 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2018-08-16 |
| Date of Report | 2018-08-16 |
| Date of Event | 2018-01-29 |
| Date Facility Aware | 2018-07-16 |
| Date Mfgr Received | 2018-07-16 |
| Date Added to Maude | 2018-08-16 |
| 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 | MS. NICOLE BROYLES |
| Manufacturer Street | 615 LAMBERT POINTE DRIVE |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| 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 | 3 |
| Brand Name | KOCHER-OCHSNER FORCEPS STR 1X2 225MM |
| Generic Name | HEMOSTAT |
| Product Code | HRQ |
| Date Received | 2018-08-16 |
| Model Number | BH648R |
| Catalog Number | BH648R |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| 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. Required No Informationntervention | 2018-08-16 |