ALPHAMAXX mobile operating table 113322F5Recalls & reported problems
MAQUET GmbH · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046768040052), received between Mar 8, 2024 and Mar 8, 2024 — classified as 1 malfunction.
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.
Reports received per month
Recalls naming this device
- 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-2273-2024 · Root cause: Component design/selection · FDA record ↗
Most reported problems
Device problems
- Positioning Failure1
- Structural Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 8, 2024Positioning Failure; Structural Problem; Positioning Failure; Structural Problem
ON 29TH FEBRUARY 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 113322F5 - ALPHAMAXX SURGICAL TABLE W/AUTO DRIVE. AS IT WAS STATED, THE TABLE WAS STUCK IN THE UPPERMOST POSITION DURING PROCEDURE AND WOULD NOT MOVE. ACCORDING TO THE CUSTOMER ALLEGATION, THE POSITION PUT THE PATIENT AT RISK OF FALLING OFF TABLE. NO ADDITIONAL DETAILS REGARDING THE PERFORMED PROCEDURE AND PATIENT POSITIONING HAVE BEEN RECEIVED TO DATE. 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 MOVE THE TABLE RESULTING IN DELAY OR INTERRUPTION IN LIFE-SAVING SURGERY AND POTENTIALLY CREATING RISK OF PATIENT FALLING FROM THE TABLE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18864226 ↗
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- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.