FDA Adverse Event Injury Summary report: N

ON-Q PAIN PUMP

MDR report key: 2499518 · Received March 16, 2012

Report

Report Number
2026095-2012-00029
Event Type
Injury
Date Received
March 16, 2012
Date of Event
September 6, 2002
Report Date
February 29, 2012
Manufacturer
I-FLOW CORP
Product Code
MEB
PMA / PMN Number
K063530
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

METHOD: NO PRODUCT WAS RETURNED FOR EVAL AND INVESTIGATION. THE LOT NUMBER WAS NOT PROVIDED, THEREFORE THE DEVICE HISTORY RECORDS COULD NOT BE REVIEWED. RESULTS: THE INFO CONTAINED IS FROM LEGAL DOCUMENTS SERVED ON I-FLOW CORPORATION. THE COMPLAINT WAS OPENED SO THAT A MEDICAL DEVICE REPORT (MDR) CAN BE FILED WITH THE U.S. FOOD AND DRUG ADMINISTRATION. NO FURTHER INVESTIGATION WILL BE CONDUCTED. THE ON-Q PUMP DIRECTIONS FOR USE (DFU) CONTAIN A WARNING THAT STATES: "AVOID PLACING THE CATHETER IN JOINT SPACES. ALTHOUGH THERE IS NO DEFINITIVE ESTABLISHED CAUSAL RELATIONSHIP, SOME LITERATURE HAS SHOWN ON A POSSIBLE ASSOCIATION BETWEEN CONTINUOUS INTRA-ARTICULAR INFUSIONS (PARTICULARLY WITH BUPIVACAINE) AND THE SUBSEQUENT DEVELOPMENT OF CHONDROLYSIS." (DFU 1307011). I-FLOW HAS ALSO PREPARED A TECHNICAL BULLETIN ENTITLED "WHAT WE KNOW ABOUT CHONDROLYSIS TODAY" (1303722, REV. E). CONCLUSION: AS THIS COMPLAINT WAS CREATED FROM A LAWSUIT SERVED ON I-FLOW, NO CUSTOMER CONTACT CAN BE MADE AT THIS TIME DUE TO THE PENDING LITIGATION.

Description of Event or Problem · 1

DRUG/DILUENT: .5% MARCAINE. FILL VOLUME: 270 CC. FLOW RATE: UNK. PROCEDURE: ARTHROSCOPIC SHOULDER (RIGHT) SURGERY. CATHPLACE: INTRA-ARTICULARLY. PT ALLEGES CHONDROLYSIS FOLLOWING PLACEMENT OF THE CATHETER FOR AN I-FLOW PAINBUSTER PUMP AFTER SURGERY ON (B)(6) 2006.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ON-Q PAIN PUMP ELASTOMERIC PUMP MEB I-FLOW CORP UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 46 YR Other