Product Wiki · Recalls · U.S. FDA — Device Enforcement

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. Model numbers YG19051 and YG19262.

U.S. FDA — Device Enforcement · United States · 2014-04-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1850-2014
Date of alert: 2014-04-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Steris Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 01108340587

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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. Model numbers YG19051 and YG19262.

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