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 2020-02-06 for CLIP APPLIER FORC.SMALL 150MM 25? FB222R manufactured by Aesculap Ag.
[179498844]
Manufacturing site evaluation: investigation on-going. Additional information / investigation results will be provided in a supplemental report.
Patient Sequence No: 1, Text Type: N, H10
[179498845]
It was reported that there was an issue with clip applier. According to the customer complaint: "when the clip is applied it does ligate but on continuation of procedure clip will slip off ligated areas causing bleeding to occur. " there was no patient harm. An additional medical intervention was not necessary. The adverse malfunction is filed under (b)(4).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610612-2019-00930 |
MDR Report Key | 9677392 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-02-06 |
Date of Report | 2020-02-06 |
Date of Event | 2019-12-13 |
Date Mfgr Received | 2020-01-13 |
Device Manufacturer Date | 2018-07-19 |
Date Added to Maude | 2020-02-06 |
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 | MS KERSTIN ROTHWEILER |
Manufacturer Street | PO BOX 40 |
Manufacturer City | TUTTLINGEN, 78501 |
Manufacturer Country | GM |
Manufacturer Postal | 78501 |
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 | CLIP APPLIER FORC.SMALL 150MM 25? |
Generic Name | CARDIO-THORACIC SURGERY |
Product Code | GDO |
Date Received | 2020-02-06 |
Returned To Mfg | 2020-01-17 |
Model Number | FB222R |
Catalog Number | FB222R |
Lot Number | 52447395 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
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 | 2020-02-06 |