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

Recall Z-2539-2019 — Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment rooms. They provide localized lighting focused on the patient s body for detecting and treating disease, injury, and disability. The surgical lights may only be used in rooms used

U.S. FDA — Device Enforcement · United States · 2019-03-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2539-2019
Date of alert: 2019-03-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Communications
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 69712678

Reported risk: The back cover of the light head was insufficiently assembled and could potentially fall off the light.

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.

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