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Minuet 2 161AN8A1URecalls & reported problems

Arjohuntleigh AB · Minuet 2, Medical bed - w/Tilt · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982755597), received between May 10, 2021 and May 10, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • InjuryMay 10, 2021Detachment of Device or Device Component; Detachment of Device or Device Component

    A CUSTOMER REPRESENTATIVE REPORTED TO ARJO THAT A MINUET 2 SIDE RAILS ARE FAULTY. A STRAP CONNECTING BARS FROM WHICH SIDE RAIL WAS MADE BROKE. AS A RESULT, THE SIDE RAILS COLLAPSED AND DETACHED OF THE RAIL HOLDERS. THERE WERE NO INDICATION THAT THE ISSUED OCCURRED AT TIME FOR USE THE BED BY A PATIENT. NO INJURY WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11796316 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.