CLASS II Device recall · Reported 2 Jul 2014 · FDA Enforcement Report

Vertical Spring Arm for Single or Dual Monitor Mount recalled by Steris

Steris is recalling Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700, distributed in Massachusetts, New York, Ohio, Pennsylvania, Texas. The recall was initiated on 4 Apr 2014 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesModel #: YG19051, Serial #'s: 01108340587, 01117338881, 011106337516, 011106337525, 011106337527, 011106337534, 011106337535, 011106337538, 011106337539, 011106337541, 011106337626, 011107338878, 011107338882, 011107338883, 011108340587, 011108340600, 0111073388883 & 011108340600A. Model #: YG19262, Serial #: ART00001 - ART00010, CADS0001 - CADS0015, CBX0001 - CBX0010 & CXSG0008 - CXSG0022.

Quantity recalled68 units

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-1850-2014
FDA event ID: 68128
Recalling firm: Steris, Mentor, OH
Classification: Class II
Status: Terminated
Recall initiated: 4 Apr 2014
FDA classified: 23 Jun 2014
Reported: 2 Jul 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Device Malfunction
Device type: Surgical Instruments

Timeline

4 Apr 2014	Recall initiated by company
23 Jun 2014	Classified by FDA	+80 days
2 Jul 2014	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

Potential for the welded seam in affected monitor spring arms to crack and/or break.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700 surgical lighting systems), Steris Corporation. Model numbers YG19051 and YG19262.

Where it was distributed

Distribution to US (states: MA, NY, OH, PA & TX) and Canada.

Massachusetts New York Ohio Pennsylvania Texas

Questions about this recall

Is Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700 recalled?

Yes. Steris recalled Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700 on 4 Apr 2014. The recall is Class II and its status is Terminated. Recall number Z-1850-2014.

Why was it recalled?

Potential for the welded seam in affected monitor spring arms to crack and/or break.

Which lots are affected?

Model #: YG19051, Serial #'s: 01108340587, 01117338881, 011106337516, 011106337525, 011106337527, 011106337534, 011106337535, 011106337538, 011106337539, 011106337541, 011106337626, 011107338878, 011107338882, 011107338883, 011108340587, 011108340600, 0111073388883 & 011108340600A. Model #: YG19262, Serial #: ART00001 - ART00010, CADS0001 - CADS0015, CBX0001 - CBX0010 & CXSG0008 - CXSG0022.

Where was it sold?

Distribution to US (states: MA, NY, OH, PA & TX) and Canada.

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 21 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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