MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-03-29 for TC METZENBAUM SCISSORS DEL CVD 200MM BC275R manufactured by Aesculap Ag.
[140310840]
(b)(4). When additional information is received a follow up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
[140310841]
It was reported by the healthcare professional "that the wrong item number is on the scissors. " the product is mislabeled. All med watch submissions related to this are: 9610612-2019-00204; 9610612-2019-00205.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610612-2019-00203 |
MDR Report Key | 8464011 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-03-29 |
Date of Report | 2019-03-28 |
Date Facility Aware | 2019-03-21 |
Date Mfgr Received | 2019-03-11 |
Device Manufacturer Date | 2016-04-01 |
Date Added to Maude | 2019-03-29 |
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 | MRS. 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 | TC METZENBAUM SCISSORS DEL CVD 200MM |
Generic Name | DUROTIP SCISSORS |
Product Code | LRW |
Date Received | 2019-03-29 |
Returned To Mfg | 2019-03-12 |
Model Number | BC275R |
Catalog Number | BC275R |
Lot Number | 4507560233 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
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 | 2019-03-29 |