CLASS II Device recall · Reported 9 Nov 2016 · FDA Enforcement Report

Product Number 3102071 Ceiling Bracket, Arch 71 White recalled

Hill-Rom is recalling Product Number 3102071 Ceiling Bracket, Arch 71 White with use on ceiling installed rail, distributed in Michigan, North Carolina, Pennsylvania, Washington. The recall was initiated on 9 Aug 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesmanufacturing date between Dec 01, 2015- Apr 14, 2016

Quantity recalled188

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0326-2017
FDA event ID: 75197
Recalling firm: Hill-Rom, Batesville, IN
Classification: Class II
Status: Terminated
Recall initiated: 9 Aug 2016
FDA classified: 31 Oct 2016
Reported: 9 Nov 2016
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

9 Aug 2016	Recall initiated by company
31 Oct 2016	Classified by FDA	+83 days
9 Nov 2016	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Product as listed by the FDA

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.

Where it was distributed

WA NC OH PA MI Australia Sweden

Michigan North Carolina Pennsylvania Washington

Questions about this recall

Why was it recalled?

Which lots are affected?

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

Where was it sold?

WA NC OH PA MI Australia Sweden

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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