inforMED
InjuryKNT

CARDINAL HEALTH

Received Jul 7, 2026 · Event occurred May 15, 2026

Report 1423537-2026-00219 · MDR key 25732517

Device

Generic name

Tubes, Gastrointestinal (and Accessories)

Model number

8884721252E

Catalog number

8884721252E

Product problems

  • Detachment of Device or Device Component

Patient

NA · Unknown

  • Needle Stick/Puncture

Narrative

Description of Event or Problem

THE CUSTOMER REPORTED THE RN WENT TO REMOVE THE GUIDEWIRE FROM PATIENT'S NG TUBE WHEN THE PURPLE CAP OF THE GUIDEWIRE CAME OFF. THE WIRE UNDERNEATH THE PURPLE CAP WAS SHARP AND CUT THE RN'S FINGER, RESULTING IN A POTENTIAL BLOOD AND BODY FLUID EXPOSURE. THE GUIDEWIRE WAS STILL ABLE TO BE REMOVED AFTER CAP FAILURE. THE RN HAD TO UNDERGO BBFE PROTOCOLS/TREATMENT AND STARTED PROPHYLACTIC MEDICATIONS. PER ADDITIONAL INFORMATION PROVIDED ON 22JUN2026, BBFE (BLOOD BODY FLUID EXPOSURE) PROPHYLAXIS TREATMENT IS A STANDARD TREATMENT FOR POTENTIAL EXPOSURE TO BBFE. AT THIS TIME, THE STAFF WAS STARTED ON THIS TREATMENT, HARM LEVEL UNKNOWN.

Additional Manufacturer Narrative

AN INVESTIGATION IS CURRENTLY UNDERWAY. UPON COMPLETION THE RESULTS WILL BE FORWARDED.