[Recalled] SlingBar Standard. Designed to meet the needs for lifting humans. — Retrospective review found 4 sling bars that may present a potential for impale… | FDA 2013-04-30

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Retrospective review found 4 sling bars that may present a potential for impalement if a patient, caregiver or bystander were to fall onto the hooks based on a simulated test method. In effort to eliminate any risk of injury, Hill-Rom is requesting products be removed from field use and replaced with an updated design.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Hill-Rom, Inc.

• Steriseal-Cannula Ophthalmic; Bi-Manual Irrigating/Aspirating Handpiece. — Class II
• Viking M, L, and XL Mobile Lifts. Non-AC-powered patient lift. — Class II
• SlingBar 350. Designed to meet the needs for lifting humans. — Class II
• TotalCare SpO2RT2 bed. Product Usage: Bed, flotation therapy, powered bed may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post anesthesia care unit (PACU), and se — Class II
• Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Pe — Class II
• Liko Mobile Lifts: Primarily intended for use in nursing homes LikoM230 Model: 2050015 — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.