V. Mueller CD0-4CRecalls & reported problems
Steris Corporation · GENESIS QTR-LENGTH CONTAINER 12 X 8 inches30.5 X 20.3CM 4 inches10.2CMDEEP SOLID BOTTOM · 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 10885403018909), received between Jul 1, 2026 and Jul 1, 2026 — classified as 1 malfunction.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 1, 2026Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY (LACERATION) TO HER THUMB WHILE OPENING A GENESIS CONTAINER. IT IS UNKNOWN THE TYPE OF MEDICAL TREATMENT THAT MAY HAVE BEEN SOUGHT OR ADMINISTERED.
Patient problems: Laceration(s)
MAUDE report 25679167 ↗
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- V. Mueller CD5-3B-REDCarefusion 2200, Inc · Sterilization wrap containers, trays, cassettes & other accessories1 recall0 reports
- V. Mueller CD5-3STCarefusion 2200, Inc · Sterilization wrap containers, trays, cassettes & other accessories1 recall0 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.