Alaris 30822Recalls & reported problems
BD Switzerland Sàrl · Extension Set, 157 cm (62 in) · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613203011112), received between Dec 18, 2019 and Dec 18, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
- Fluid/Blood Leak1
- Material Split, Cut or Torn1
Patient problems
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 18, 2019Break; Fluid/Blood Leak; Material Split, Cut or Torn; Break; Fluid/Blood Leak; Material Split, Cut or Torn
THIS FILE WAS CREATED FOR AN UNSPECIFIED TUBING ISSUE IN WHICH PATIENT AND EVENT INFORMATION WERE NOT PROVIDED. ALTHOUGH REQUESTED, THERE IS NO FURTHER PATIENT OR EVENT INFORMATION AVAILABLE.
Patient problems: No Consequences Or Impact To Patient; No Information
MAUDE report 9489470 ↗
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- Autosoft XC 1001681Unomedical A/S · Set, Administration, Intravascular1 death4,216 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.