Hill-Rom, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0326-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likorall 200, 242, 243, 250, and LikoGuard L and XL.

Product Classification:

Class II

Date Initiated: August 9, 2016

Date Posted: November 9, 2016

Recall Number: Z-0326-2017

Event ID: 75197

Reason for Recall:

Ceiling Bracket 71 was shipped with a larger center hole. A potentially hazardous situation exists that if the Ceiling Bracket 71 with a larger center hole is used for a concrete ceiling Ultra System installation with the M8 screw and the safe working load is exceeded, the system could fall.

Status: Terminated

Product Quantity: 188

Code Information:

manufacturing date between Dec 01, 2015- Apr 14, 2016

Distribution Pattern:

WA NC OH PA MI Australia Sweden

Voluntary or Mandated:

Voluntary: Firm initiated