NA FD107Recalls & reported problems
Corporation Steris Canada · The Three Level Manifold Long Rack is multi-functional and is designed to hold a maximum of 6 trays of surgical instruments and hard goods on each level. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995150969), received between Jul 12, 2022 and May 1, 2026 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
- Use of Device Problem1
Patient problems
- Laceration(s)2
- Burn(s)1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 1, 2026Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT EMPLOYEES SUSTAINED CUTS TO THEIR HANDS WHILE HANDLING THEIR THREE LEVEL MANIFOLD RACKS. IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Laceration(s)
MAUDE report 25057124 ↗MalfunctionDec 23, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A BURN ON THEIR HAND WHILE TRYING TO UNLOAD A THREE LEVEL MANIFOLD RACK FROM THEIR WASHER. THE EMPLOYEE DID NOT SEEK MEDICAL TREATMENT AND RETURNED TO WORK.
Patient problems: Burn(s)
MAUDE report 21004270 ↗InjuryJul 12, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A CUT TO THEIR FINGER WHILE MANUALLY PULLING A MANIFOLD RACK OUT OF THEIR WASHER. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT (STITCHES).
Patient problems: Laceration(s)
MAUDE report 14986911 ↗
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- AMSCO 7052HPCorporation Steris Canada · Disinfector, medical devices1 recall10 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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