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
Manufacturer
Medline Industires, Lp- NamicCatalog 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