RecallRadar

FDA Device recall Z-1850-2014

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

On 2014-07-02 the FDA classified a Class II recall of Vertical Spring Arm for Single or Dual Monitor Mount (Harmony LL 500 and Harmony LL 700 surgical lighting systems), Steris Corporation by Steris, citing potential for the welded seam in affected monitor spring arms to crack and/or break.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1850-2014
ClassificationClass II
Statusterminated
Initiated2014-04-04
Published2014-07-02
Last updated2026-09-13 11:53 UTC
CompanySteris
DistributionMA, NY, OH, PA, TX

Product

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.

Reason

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

Identifiers

code_info
Model #: YG19051, Serial #'s: 01108340587, 01117338881, 011106337516, 011106337525, 011106337527, 011106337534, 0111063…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.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1850-2014%22

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