FDA Adverse Event Malfunction Summary report: N

HUDSON AQUAPAK 301 SW,340 ML,INTL

MDR report key: 5111175 · Received September 29, 2015

Report

Report Number
1417411-2015-00159
Event Type
Malfunction
Date Received
September 29, 2015
Date of Event
September 1, 2015
Report Date
September 22, 2015
Manufacturer
TELEFLEX MEDICAL
Product Code
BTT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A VISUAL, FUNCTIONAL AND DIMENSIONAL INSPECTION OF THE PRODUCT INVOLVED IN THE COMPLAINT COULD NOT BE CONDUCTED SINCE THE PRODUCT WAS NOT RECEIVED AT OUR FACILITY. BASED ON THE LOT # 038157 PROVIDED FOR WHICH THE DHR RESIDES AT ARLINGTON HEIGHTS FACILITY, THE (B)(4) LOT NUMBERS FOR COMPONENT (B)(4) WERE OBTAINED. RECORDS REVIEWED SHOWED THAT THERE WERE NO ISSUES RELATED TO FUNCTIONAL ISSUES ON THE MOLDED COMPONENT INVOLVED IN THIS COMPLAINT (B)(4) (SNAP-ON FLOWMETER ADAPTOR) BATCH # 4-091422, 5-091421, 5-091422, 6-091421, 6-091422, 7-091421 & 7-091422 DURING THE MANUFACTURE OF THE MATERIAL. CUSTOMER COMPLAINT CANNOT BE CONFIRMED, BASED ONLY ON THE INFORMATION PROVIDED, TO PERFORM A CORRECT INVESTIGATION AND DETERMINE THE SOURCE OF DEFECT REPORTED IT IS NECESSARY TO EVALUATE THE SAMPLE INVOLVED IN THIS COMPLAINT. REGARDING OTHER CUSTOMER COMPLAINTS FROM THIS SAME ISSUE, A CAPA FILE #(B)(4) WAS OPENED TO PERFORM A FURTHER INVESTIGATION FOR THIS ISSUE. ACCORDING TO THE CAPA INVESTIGATION SO FAR THE ROOT CAUSE FOR THE ISSUE WAS THE POSITIONING OF THE THREAD LEAD AND THE SOFTNESS OF THE NEW RESIN USED FOR THE SNAP ADAPTOR. IF DEVICE SAMPLE BECOMES AVAILABLE AT A LATER DATE THIS COMPLAINT WILL BE RE-OPENED.

Description of Event or Problem · 1

THE CUSTOMER ALLEGES BUBBLING WHEN CONNECTED BETWEEN THE SNAP CAP AND THE OXYGEN OUTLET.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
641331 HUDSON AQUAPAK 301 SW,340 ML,INTL HUMIDIFIER BTT TELEFLEX MEDICAL 038157

Patients

Seq Age Sex Outcome Treatment
1