MalfunctionOIB
MEDLINE
Received Jul 2, 2026 · Event occurred Jun 2, 2026
Report 3004519921-2026-00032 · MDR key 25699599
Device
Generic name
Blood Culture Kit
Manufacturer
Tri-state De Mexico, S. De R.l. De C.vCatalog number
DYNDH1906C
Lot number
2026031290
Product problems
- Obstruction of Flow
- Material Twisted/Bent
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
IT WAS REPORTED THAT THE TUBE WAS BENT, NOT ALLOWING BLOOD TO FLOW.
Additional Manufacturer Narrative
IT WAS REPORTED THAT THE TUBE WAS BENT, NOT ALLOWING BLOOD TO FLOW. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED.