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V. Mueller SU2856Recalls & reported problems

Steris Corporation · V. Mueller TUBING CLAMP FORCEPS TUBING MAX O.D. 7/8 inches 22MM withWALL 3/32 inches TO 1/8 inches OVERALL LENGTH 8 inches 20.3CM · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403064746), received between Jan 31, 2023 and Jan 31, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fluid/Blood Leak1

Patient problems

  • Hemorrhage/Blood Loss/Bleeding1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryJan 31, 2023Fluid/Blood Leak; Fluid/Blood Leak

    MATERIAL NO: SU2856 BATCH NO: D22XMR. IT WAS REPORTED BY THE CUSTOMER THAT THE INSTRUMENTS ARE BOWED/HAVE A GAP THAT IS NOT ACCEPTABLE FOR CATH LAB. VERBATIM: IN REGARDS TO THE PATIENT ¿THAT HAD SUCH HIGH PRESSURES IT WAS VERY NOTICEABLE THE CLAMP DID NOT MEET STANDARDS. THIS EVENT IS RELATED TO ONE PATIENT. WE WERE NOT ABLE TO OCCLUDE THE CANNULAS THUS LOOSING BLOOD". NO FURTHER INFORMATION AVAILABLE.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 16273590 ↗

Other CLAMP devices

All CLAMP devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.