Medical device recalls Moderate risk

Hill-Rom, Inc. recalls Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail systems: Multirall 200, Likora…

Recall date
August 9, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0326-2017
FDA classification
Class II
Brand / firm
Hill-Rom, Inc.
Sold / distributed
WA NC OH PA MI Australia Sweden

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

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