ALPHAMAXX mobile operating table 113322B4Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04046768040007), received between Mar 3, 2023 and Mar 7, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. May 29, 2024Open, Classified

   The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.

   Z-2271-2024 · Root cause: Component design/selection · FDA record ↗

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 7, 2024Positioning Failure; Positioning Failure

  ON 28TH FEBRUARY 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 113322B4 - ALPHAMAXX (460 MM LONGIT. SHIFT), EU. AS IT WAS STATED, A SURGEON COULD NOT CONTROL THE TABLE DURING ORTHOPEDIC CASE WITH X-RAY C-ARM ON ANESTHETIZED PATIENT. ERROR LIGHT WAS SHOWN ON LOCK AND UNLOCK BUTTON AND TABLE COULD NOT BE ADJUSTED (HEIGHT, ZERO POSITION, LEFT TILT FUNCTIONS). THE SURGERY WAS DELAYED AND SURGEON HAD TO WAIT FOR 30 MINUTES TO TRANSFER THE PATIENT FROM ALPHAMAXX TO OTHER TABLE IN ANOTHER OPERATING ROOM. THE PROCEDURE WAS CONTINUED AND FINISHED IN DIFFERENT OPERATING ROOM. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE INABILITY TO POSITION THE PATIENT AS REQUIRED AND A DELAY RESULTING IN PROLONGED ANESTHESIA TIME, WERE TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18855409 ↗
• MalfunctionMar 3, 2023Use of Device Problem; Use of Device Problem

  MANUFACTURER'S REFERENCE NUMBER (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16476452 ↗