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[Recalled] Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital. — During an evaluation of Advanta 2 siderail samples returned from the field it w… | FDA 2012-06-18

recall fda device united-states

Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.

Recall details

ProductAdvanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.
Brand / manufacturerHill-Rom, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1864-2012
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date18 June 2012

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: During an evaluation of Advanta 2 siderail samples returned from the field it was found that the screws used to attach the siderail were being stripped from the plastic cavity of the siderail.

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.

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.

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