MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2010-09-09 for CLOSED KNOT PUSHER N/A 902813 manufactured by Biomet Sports Medicine, Inc..
[1704506]
It was reported that patient underwent a procedure utilizing a closed knot pusher on (b)(6) 2010. During the procedure, the knot pusher cut a suture. An additional suture was implanted, but the knot pusher cut that one as well. The procedure was completed using a competitor's knot pusher.
Patient Sequence No: 1, Text Type: D, B5
[8702698]
Closed knot pusher part 902813 lot 864100 subject of recall. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1825034-2010-00364 |
MDR Report Key | 1829334 |
Report Source | 07 |
Date Received | 2010-09-09 |
Date of Report | 2010-08-13 |
Date of Event | 2010-08-11 |
Date Facility Aware | 2010-09-01 |
Date Mfgr Received | 2010-08-13 |
Device Manufacturer Date | 2010-03-29 |
Date Added to Maude | 2010-09-09 |
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 | 0 |
Event Location | 3 |
Manufacturer Contact | MR. JEREMY SCHROEDER |
Manufacturer Street | 56 E. BELL DRIVE P.O. BOX 587 |
Manufacturer City | WARSAW IN 46581 |
Manufacturer Country | US |
Manufacturer Postal | 46581 |
Manufacturer Phone | 5743713755 |
Manufacturer G1 | BIOMET SPORTS MEDICINE, INC. |
Manufacturer Street | 56 E. BELL DRIVE P.O. BOX 587 |
Manufacturer City | WARSAW IN 46581 |
Manufacturer Country | US |
Manufacturer Postal Code | 46581 |
Single Use | 3 |
Remedial Action | RC |
Previous Use Code | 3 |
Removal Correction Number | RES # 56589 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLOSED KNOT PUSHER |
Generic Name | PUSHER, SOCKET |
Product Code | HXO |
Date Received | 2010-09-09 |
Returned To Mfg | 2010-08-20 |
Model Number | N/A |
Catalog Number | 902813 |
Lot Number | 864100 |
Operator | PHYSICIAN |
Device Availability | R |
Device Age | 4 MO |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMET SPORTS MEDICINE, INC. |
Manufacturer Address | 56 E. BELL DRIVE P.O. BOX 587 WARSAW IN 46581 US 46581 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2010-09-09 |