FDA Adverse Event Summary report: N

SUCTION CATHETER KIT, 8 FR

MDR report key: 14652 · Received July 13, 1994

Report

Report Number
MW1002798
Date Received
July 13, 1994
Date of Event
June 1, 1994
Report Date
June 30, 1994
Manufacturer
SUPERIOR HEALTHCARE GROUP, INC.
Product Code
BSY
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
RESPIRATORY THERAPIST

Narratives

Description of Event or Problem · 1

SUCTION CATHETER IS USED EXCLUSIVELY IN THE NICU. PROBLEM: FLAT AREA NEAR THE TIP OF THE CATHETER PREVENTS INSERTION OF THE CATHETER AND IF THE CATHETER CAN BE INSERTED, IT IS DIFFICULT TO REMOVE. MULTIPLE INCIDENTS. (*)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SUCTION CATHETER KIT, 8 FR BSY SUPERIOR HEALTHCARE GROUP, INC. 4050 A

Patients

Seq Age Sex Outcome Treatment
1 *