MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,user facility report with the FDA on 2014-01-08 for OSTRUM ANTRUM PUNCH BACKBITER RT 1/EA 3712034 manufactured by Medtronic Xomed, Inc..
[19925934]
It was reported that during a fess procedure, the instrument broke in the patient's nose. A small piece was retrieved from the patient during the procedure and the surgery was successfully completed.
Patient Sequence No: 1, Text Type: D, B5
[20179941]
(b)(4). This device is used for therapeutic purposes. Product evaluation: no analysis results available; device has not been returned. Method: no testing methods performed.
Patient Sequence No: 1, Text Type: N, H10
[101909111]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1045254-2014-00010 |
MDR Report Key | 3561081 |
Report Source | 06,USER FACILITY |
Date Received | 2014-01-08 |
Date of Report | 2013-12-18 |
Date of Event | 2013-12-16 |
Date Mfgr Received | 2013-12-18 |
Device Manufacturer Date | 2013-03-01 |
Date Added to Maude | 2014-04-09 |
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 | MICHELLE ALFORD |
Manufacturer Street | 6743 SOUTHPOINT DRIVE NORTH |
Manufacturer City | JACKSONVILLE FL 32216 |
Manufacturer Country | US |
Manufacturer Postal | 32216 |
Manufacturer Phone | 9043328197 |
Manufacturer G1 | MEDTRONIC XOMED, INC. |
Manufacturer Street | 6743 SOUTHPOINT DRIVE NORTH |
Manufacturer City | JACKSONVILLE FL 32216 |
Manufacturer Country | US |
Manufacturer Postal Code | 32216 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OSTRUM ANTRUM PUNCH BACKBITER RT 1/EA |
Generic Name | PUNCH, NASAL |
Product Code | KAY |
Date Received | 2014-01-08 |
Model Number | 3712034 |
Catalog Number | 3712034 |
Lot Number | 13031 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC XOMED, INC. |
Manufacturer Address | 6743 SOUTHPOINT DRIVE NORTH JACKSONVILLE FL 32216 US 32216 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-01-08 |