FDA Adverse Event Injury Summary report: N

GARG

MDR report key: 1673806 · Received April 24, 2010

Report

Report Number
1320894-2010-00056
Event Type
Injury
Date Received
April 24, 2010
Report Date
April 23, 2010
Manufacturer
CONMED CORPORATION
Product Code
KDQ
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VT, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

A REVIEW OF THE MFG DOCUMENTS FROM THE DHR/LHR FOR LOT 0810031 HAS VERIFIED THE DEVICES WERE PRODUCED ACCORDING TO CURRENT AND APPROVED PROCEDURES AND MATERIAL SPECIFICATIONS. NON-CONFORMANCES REGARDING THE PRODUCT'S IDENTITY, QUALITY, SAFETY, EFFECTIVENESS OR PERFORMANCE WERE NOT IDENTIFIED DURING MANUFACTURE. NO LABORATORY EXAMINATION WAS PERFORMED ON THE COMPLAINT PRODUCTS, AS NO DEVICES WERE MADE AVAILABLE. COMPLAINT HISTORY HAS SHOWN SIMILAR COMPLAINTS, HOWEVER, WITHOUT THE DEVICE WE CANNOT CONFIRM ANY MFG DEFECTS. THERE MAY BE A MULTIPLE OF POSSIBLE CAUSES, EITHER MFG OR USER RELATED, FOR THIS COMPLAINT. THE COMPLAINT CAN BE NEITHER CONFIRMED NOR UNCONFIRMED AT THIS TIME. IF THE PRODUCT IS RETURNED IN THE FUTURE, THE COMPLAINT WILL BE RE-OPENED AND A FURTHER INVESTIGATION WILL BE PERFORMED. NO CORRECTIVE ACTION CAN BE RECOMMENDED AT THIS TIME. WE ARE CONSIDERING THIS COMPLAINT CLOSED. THIS REPORT IS LINKED TO THE FOLLOWING MEDWATCHES: 1320894-2010-00046; -00054; AND -00055.

Description of Event or Problem · 1

IT WAS REPORTED, "FOUR DIFFERENT NEEDLES, SAME PT WERE USED AND LEAKED. THE PT HAD TO HAVE A CHEST TUBE PLACED IN CHEST." CAT. #THR-1720. THIS OCCURRED OVER THE WEEKEND OF (B) (6) 2010; END-USER DID NOT HAVE THE EXACT DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GARG THORACENTESIS NEEDLE KDQ CONMED CORPORATION NA 0810031

Patients

Seq Age Sex Outcome Treatment
1 UNK Required Intervention