Atlas AX0660230830000013Recalls & reported problems
Steris Mexico, S. de R.L. de C.V. · The Atlas Transfer Carriage 26x37.5x60-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
- 9
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00724995150631), received between Dec 8, 2022 and Apr 10, 2026 — classified as 9 malfunctions.
The most frequently reported specific device problem is “Failure to Align” (4 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
- Failure to Align4
- Device Dislodged or Dislocated3
- Device Handling Problem1
- Use of Device Problem1
Patient problems
- Burn(s)2
- Laceration(s)2
- Pain2
- Hyperextension1
- Insufficient Information1
- Muscle/Tendon Damage1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 10, 2026Failure to Align
THE USER FACILITY REPORTED AN EMPLOYEE OBTAINED AN INJURY TO THEIR SHOULDER WHILE ATTEMPTING TO REMOVE THE ATLAS TRANSFER CARRIAGE FROM THE STERILIZER. THE EMPLOYEE SOUGHT MEDICAL TREATMENT; HOWEVER, IT IS UNKNOWN WHAT MEDICAL TREATMENT WAS ADMINISTERED.
Patient problems: Pain
MAUDE report 24845361 ↗MalfunctionJan 29, 2026Failure to Align
THE USER FACILITY REPORTED THAT AN EMPLOYEE EXPERIENCED BACK AND THIGH PAIN AND DISCOMFORT AFTER UNLOADING THEIR ATLAS TRANSFER CARRIAGE. IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Pain
MAUDE report 24215396 ↗MalfunctionNov 21, 2025Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A BURN ON THEIR ARM AFTER STRUGGLING TO UNLATCH THE ATLAS TRANSFER CARRIAGE FROM THEIR STERILIZER. THE EMPLOYEE RECEIVED BURN CREAM AND A BANDAGE AND RETURNED TO WORK.
Patient problems: Burn(s)
MAUDE report 23621683 ↗MalfunctionJun 5, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A SMALL CUT ON THEIR HAND WHILE OPERATING THEIR ATLAS TRANSFER CARRIAGE. THE EMPLOYEE SELF-TREATED BY APPLYING A BANDAGE.
Patient problems: Laceration(s)
MAUDE report 22154258 ↗MalfunctionDec 19, 2024Failure to Align; Failure to Align
THE USER FACILITY REPORTED THAT AN EMPLOYEE SUSTAINED A MUSCLE STRAIN IN THEIR SHOULDER WHILE UNLOADING THEIR LOADING CAR. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED (FIRST AID).
Patient problems: Muscle/Tendon Damage
MAUDE report 20976597 ↗MalfunctionAug 9, 2024Device Handling Problem; Device Handling Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS INJURED WHILE MOVING THEIR ATLAS TRANSFER CARRIAGE. NO REPORT OF PROCEDURE DELAY. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED (SURGERY).
Patient problems: Hyperextension
MAUDE report 19950106 ↗MalfunctionJul 23, 2024Failure to Align; Failure to Align
THE USER FACILITY REPORTED THAT AN EMPLOYEE INJURED THEIR SHOULDER WHILE OPERATING AN ATLAS TRANSFER CARRIAGE. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED. IT IS UNKNOWN WHAT TYPE OF MEDICAL TREATMENT WAS ADMINISTERED.
Patient problems: Insufficient Information
MAUDE report 19810636 ↗MalfunctionJun 5, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY TO THEIR HAND (LACERATION) WHILE OPERATING THEIR ATLAS TRANSFER CARRIAGE. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED (SKIN ADHESIVE).
Patient problems: Laceration(s)
MAUDE report 19472905 ↗MalfunctionDec 8, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE USER FACILITY REPORTED THAT THEIR ATLAS TRANSFER CARRIAGE DID NOT STAY ENGAGED WITHIN THE STERILIZER AND SUBSEQUENTLY CONTACTED AN EMPLOYEE. THE EMPLOYEE OBTAINED A BURN AND APPLIED A BAND-AID.
Patient problems: Burn(s)
MAUDE report 15943369 ↗
Other Sterilizer, steam devices
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- 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
- 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
- AMSCO AMSCO 400 Steam SterilizerSteris Mexico, S. de R.L. de C.V. · Sterilizer, steam7 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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