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

Recall Z-2311-2012 — Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puchheim. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.

U.S. FDA — Device Enforcement · United States · 2012-05-29 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2311-2012
Date of alert
2012-05-29
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Trumpf Medical Systems, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
011201602557
Reported risk: Cracks can arise on the welded seam on the rear joint.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.