Atlas AX0650230830000013Recalls & reported problems
Steris Mexico, S. de R.L. de C.V. · The Atlas Transfer Carriage 26-inch x 37.5-inch x 48-inch (for Hinged Door Only) is designed for use with the sterilization systems. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995150600), received between Aug 22, 2024 and Mar 6, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Use of Device Problem” (2 reports).
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
- Use of Device Problem2
Patient problems
- Pain2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2026Use of Device Problem
THE USER FACILITY REPORTED THAT AN INSTRUMENT RACK UNLOADED AT AN ANGLE ON THE CART OF THEIR ATLAS TRANSFER CARRIAGE. THE EMPLOYEE ATTEMPTED TO MANUALLY LIFT THE RACK AND SUBSEQUENTLY PINCHED THEIR FINGER BETWEEN THE RACK AND CARRIAGE. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED.
Patient problems: Pain
MAUDE report 24530934 ↗MalfunctionAug 22, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY TO THEIR BACK WHILE LOADING THEIR ATLAS TRANSFER CARRIAGE INTO A AMSCO 400 STEAM STERILIZER. THE USER FACILITY DID NOT DISCLOSE INFORMATION REGARDING THE REPORTED INJURY HOWEVER, NO MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Pain
MAUDE report 20043030 ↗
Other Sterilizer, steam devices
- NA P2131-2Fort Defiance Industries, LLC · Sterilizer, Steam1 recall0 reports
- STATCLAVE G4 Chamber Autoclave G4-621103Scican Ltd · Sterilizer, Steam1 recall0 reports
- STATCLAVE G4 Chamber Autoclave G4-622303Scican Ltd · Sterilizer, Steam1 recall0 reports
- NA AX083020003Steris Mexico, S. de R.L. de C.V. · Sterilizer, steam23 reports
- AMSCO AMSCO 400 Steam SterilizerSteris Mexico, S. de R.L. de C.V. · Sterilizer, steam11 reports
- Atlas AX0660230830000013Steris Mexico, S. de R.L. de C.V. · Sterilizer, steam9 reports
- AMSCO AMSCO 400 Steam SterilizerSteris Mexico, S. de R.L. de C.V. · Sterilizer, steam9 reports
- AMSCO AMSCO 600 Steam SterilizerSteris Mexico, S. de R.L. de C.V. · Sterilizer, steam8 reports
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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