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 2017-07-31 for 3/4-SIZE LID W/RETENTION PLATE SILVERSTERILE TECHNOLOGY JK789 manufactured by Aesculap Ag.
[81433746]
(b)(4). Manufacturing site evaluation: evaluation on-going.
Patient Sequence No: 1, Text Type: N, H10
[81433747]
Country of complaint: (b)(6). It has been reported that fluff (dark in color) was found inside the containers that have been sterilized. Components in use listed as concomitant devices are: jk789 / 3/4-size lid w/retention plate silver. Jk740 / bottom for 3/4 container height: 90 mm.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9610612-2017-00388 |
| MDR Report Key | 6754356 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2017-07-31 |
| Date of Report | 2017-07-31 |
| Date of Event | 2017-06-02 |
| Date Facility Aware | 2017-07-24 |
| Date Mfgr Received | 2017-07-10 |
| Date Added to Maude | 2017-07-31 |
| 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 | 3/4-SIZE LID W/RETENTION PLATE SILVERSTERILE TECHNOLOGY |
| Generic Name | STERILE TECHNOLOGY |
| Product Code | FRG |
| Date Received | 2017-07-31 |
| Model Number | JK789 |
| Catalog Number | JK789 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| 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 | 2017-07-31 |