MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2020-03-11 for ORTHOPEDIATRICS 3.2MM CANNULATED DRILL, SHORT N/A 01-1400-0017 manufactured by Orthopediatrics, Inc.
Report Number | 3006460162-2020-00043 |
MDR Report Key | 9820538 |
Report Source | DISTRIBUTOR,HEALTH PROFESSION |
Date Received | 2020-03-11 |
Date of Report | 2020-03-11 |
Date of Event | 2020-02-11 |
Date Mfgr Received | 2020-02-11 |
Device Manufacturer Date | 2018-08-01 |
Date Added to Maude | 2020-03-11 |
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 | KRISS ANDERSON |
Manufacturer Street | 2850 FRONTIER DRIVE |
Manufacturer City | WARSAW, IN |
Manufacturer Country | US |
Manufacturer Phone | 2670872 |
Manufacturer G1 | ORTHOPEDIATRICS, INC |
Manufacturer Street | 2850 FRONTIER DRIVE |
Manufacturer City | WARSAW, IN |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ORTHOPEDIATRICS 3.2MM CANNULATED DRILL, SHORT |
Generic Name | BIT, SURGICAL |
Product Code | GFG |
Date Received | 2020-03-11 |
Returned To Mfg | 2020-02-20 |
Model Number | N/A |
Catalog Number | 01-1400-0017 |
Lot Number | 91902437-C |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ORTHOPEDIATRICS, INC |
Manufacturer Address | 2850 FRONTIER DRIVE WARSAW, IN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-11 |