FDA Adverse Event Malfunction Summary report: N

ESY-TAP LEG BG W/18 PVC TUBING

MDR report key: 12149101 · Received July 12, 2021

Report

Report Number
3011137372-2021-00192
Event Type
Malfunction
Date Received
July 12, 2021
Date of Event
June 17, 2021
Report Date
June 18, 2021
Manufacturer
TELEFLEX MEDICAL
Product Code
FAQ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). TELEFLEX WILL CONTINUE TO MONITOR AND TREND RELATED EVENTS.

Description of Event or Problem · 1

SHE DOES NOT LIKE THE BAGS WE SENT BECAUSE THEY CAUSE AN INFECTION ON HER SKIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1046588 ESY-TAP LEG BG W/18 PVC TUBING ESY-TAP LEG BG W/18 PVC TUBING FAQ TELEFLEX MEDICAL UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1