CENTROVENA ONE
Received May 6, 2026 · Event occurred Apr 20, 2026
Report 3006260740-2026-03205 · MDR key 25104154
Device
Generic name
Central Venous Catheterization Kit, Short-term
Manufacturer
C.r. Bard, Inc. (basd) -3006260740Model number
N/ACatalog number
1MC0R7320
Lot number
UNKNOWN
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Needle Stick/Puncture
Narrative
Additional Manufacturer Narrative
H11: SECTION A THROUGH F - THE INFORMATION PROVIDED BY BD REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO BD. THE DEVICE HAS NOT BEEN RECEIVED BY THE MANUFACTURER FOR EVALUATION. EACH EVENT REPORTED TO BD IS EVALUATED AND INVESTIGATED IN ACCORDANCE WITH OUR COMPLAINT INVESTIGATION PROCEDURES. THE INVESTIGATION PROCESS INCLUDES, BUT IS NOT LIMITED TO, EVALUATION OF THE EVENT DETAILS PROVIDED BY THE COMPLAINT FACILITY, A REVIEW OF COMPLAINT HISTORY, MANUFACTURING RECORDS AND RISK DOCUMENT WHERE APPLICABLE, AND AN EVALUATION OF THE SUBJECT DEVICE WHEN AVAILABLE TO IDENTIFY POTENTIAL CONTRIBUTING FACTORS.
Description of Event or Problem
IT WAS REPORTED NEEDLE STICK WHEN PLACING SUTURES. CLINICIAN WAS SENT FOR FOLLOW UP ACCORDING TO THEIR POLICY. PATIENT DID NOT HAVE ANY BLOOD BORNE DISEASES, AND NO ADVERSE EVENT OR SERIOUS INJURY TO PATIENT OR HEALTHCARE PROVIDER.