MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2014-11-03 for ULTRASONIC PROBE 27093LL manufactured by Karl Storz Gmbh & Co..
[5226285]
Allegedly, during a percutaneous nephrolithotomy procedure on (b)(6) 2014, the tip of the ultrasonic probe fell off inside the patient's kidney; the surgeon was able to remove it with a grasper. Procedure was completed with no injury to patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9610617-2014-00054 |
MDR Report Key | 4268572 |
Report Source | 05,06 |
Date Received | 2014-11-03 |
Date of Report | 2014-10-02 |
Date of Event | 2014-10-02 |
Date Added to Maude | 2014-11-26 |
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 | 0 |
Manufacturer Contact | SUSIE CHEN |
Manufacturer Street | 2151 E. GRAND AVE |
Manufacturer City | EL SEGUNDO CA 902455017 |
Manufacturer Country | US |
Manufacturer Postal | 902455017 |
Manufacturer Phone | 4242188201 |
Manufacturer G1 | KARL STORZ GMBH & CO. KG |
Manufacturer Street | MITTELSTRASSE 8 |
Manufacturer City | TUTTLINGEN |
Manufacturer Country | GM |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ULTRASONIC PROBE |
Generic Name | ULTRASONIC PROBE |
Product Code | FEO |
Date Received | 2014-11-03 |
Model Number | 27093LL |
Catalog Number | 27093LL |
Lot Number | 46360 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | KARL STORZ GMBH & CO. |
Manufacturer Address | TUTTLINGEN GM |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2014-11-03 |