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Medline FCEQRSIDERecalls & reported problems

Medline Industries, Inc. · ALTERRA QUICK RELEASE SIDE RAILS · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884389104507), received between Jan 29, 2019 and Mar 3, 2020 — classified as 2 injuries.

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

  • Adverse Event Without Identified Device or Use Problem1
  • Detachment of Device or Device Component1

Patient problems

  • Skull Fracture1
  • Suture Abrasion1

Recent adverse event reports

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

  • InjuryMar 3, 2020Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE CUSTOMER WAS TRANSFERRING FROM THE BED AND CUT THEIR LEG ON THE SIDE RAIL REQUIRING SUTURES.

    Patient problems: Suture Abrasion

    MAUDE report 9782314 ↗
  • InjuryJan 29, 2019Detachment of Device or Device Component

    IT WAS REPORTED THAT A PATIENT WAS USING THE SIDE RAIL TO GET UP AND THE SIDE RAIL CAME OFF WHICH MAY HAVE RESULTED IN A PATIENT FALL.

    Patient problems: Skull Fracture

    MAUDE report 8286888 ↗

Other BED, AC-POWERED ADJUSTABLE HOSPITAL devices

All BED, AC-POWERED ADJUSTABLE HOSPITAL devices →

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