inforMED
MalfunctionDXT

NAMIC

Received Feb 25, 2026 · Event occurred Jan 28, 2026

Report 3015910259-2026-00049 · MDR key 24447171

Device

Generic name

Syringe,10ml,angio,w/ra,-,oem

Catalog number

80085007

Lot number

0000156801

Product problems

  • Connection Problem

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

ACCORDING TO THE FACILITY, SYRINGE FELL OFF MANIFOLD DURING PREPARATION. MANIFOLD AND SYRINGE STILL NOT CONNECTION ON SECOND ATTEMPT. OPENED NEW "TRIAL" SYRINGE WHICH WORKED. NO ADDITIONAL INFORMATION AT THIS TIME. TO DATE, NO INFORMATION HAS BEEN RECEIVED TO INDICATE THAT A USER OR A PATIENT EXPERIENCED A DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, FOLLOW-UP CARE, OR OTHER ADVERSE HEALTH IMPACT ASSOCIATED WITH THE REPORTED PROBLEM/ISSUE. IN AN ABUNDANCE OF CAUTION, AND IN RESPONSE TO AN FDA 483 ISSUED FOR CFN 1417592 ON 22-JAN-2024, THIS MEDWATCH IS BEING FILED FOR THE REPORTED PROBLEM/ISSUE. IF ADDITIONAL RELEVANT INFORMATION BECOMES AVAILABLE A SUPPLEMENTAL MEDWATCH WILL BE FILED.

Description of Event or Problem

ACCORDING TO THE FACILITY, SYRINGE FELL OFF MANIFOLD DURING PREPARATION.

Additional Manufacturer Narrative

UPDATED H6: INVESTIGATION FINDINGS (C). UPDATED H6: INVESTIGATION CONCLUSIONS (D). UPDATED H7: IF REMEDIAL ACTION INITIATED, CHECK TYPE. UPDATED H9: IF ACTION REPORTED TO FDA UNDER 21 USC 360I(G), LIST CORRECTION/REMOVAL REPORTING NUMBER.

Remedial action

  • Recall