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MEDLINE MDSMPHS3Recalls & reported problems

Medline Industries, Inc. · SLING,USHAPED,PAD,HDSUP,450 LB,LRG, EA · Class 1

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 10888277177673), received between Aug 22, 2022 and Aug 22, 2022 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 22, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ACCORDING TO THE FACILITY ON (B)(6) 2022 WHILE TRANSFERRING A PATIENT FROM THEIR BED TO THEIR CHAIR THE SLING STRAPS SNAPPED AND THE PATIENT FELL ONTO THE TILE FLOOR. PER THE FACILITY, 911 WAS CALLED AND THE PATIENT WAS TRANSFERRED TO THE EMERGENCY ROOM WHERE THEY PERFORMED IMAGING ON THE PATIENT'S HIPS, PELVIS, ELBOW, RIBS, AND CHEST. ACCORDING TO THE FACILITY THE IMAGING SHOWED A FRACTURE OF THE '8TH RIB'.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 15272538 ↗

Other Lift, patient, non-ac-powered devices

All Lift, patient, non-ac-powered devices →

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