Hill-Rom, Inc.: Medical Device Recall in 2012 - (Recall #: Z-1864-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Advanta 2 Bed. The Advanta 2 Bed is intended for low to moderate acuity patients in the medical/surgical area of the hospital.

Product Classification:

Class II

Date Initiated: June 18, 2012

Date Posted: July 4, 2012

Recall Number: Z-1864-2012

Event ID: 62331

Reason for Recall:

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.

Status: Terminated

Product Quantity: 7843 devices

Code Information:

AdvantaTM 2 beds (P1190) produced between August 10, 2009 and October 6, 2011; bed S/N between K222AT9180 and M279AT4403

Distribution Pattern:

Worldwide Distribution-USA (nationwide) and the countries of Canada, France, and Singapore.

Voluntary or Mandated:

Voluntary: Firm initiated