The Recall Desk
HighFDA (Devices)·Z-2356-2015·Announced 2015-08-19

Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Joint Breakage Risk

Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a structural component (spring arm joint) that could break, posing a risk of harm to patients or staff, although no injuries or fatalities are reported in the source text.

Plain-English summary

Trumpf Medical Systems, Inc. is recalling 9,287 units of Trumpf Ceiling Mounted Surgical Lighting Systems, specifically the TruVidia SD model. The recall is due to complaints that the front joint of the spring arm AC 2000 could break at the interface to the monitor.

The affected products were distributed worldwide, including the United States (nationwide) and Puerto Rico, as well as numerous countries across Europe, Asia, Africa, and the Americas. The specific material numbers associated with the recalled units are listed in the official recall documentation.

Consumers and healthcare facilities should stop using the affected surgical lighting systems immediately. Users should contact Trumpf Medical Systems, Inc. for instructions on how to resolve the issue, which may involve repair or replacement of the affected components.

The recalled product

Product
Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia SD, User Manual #1400191. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
Manufacturer
Trumpf Medical Systems, Inc.
Category
Medical Device — Surgical Lighting
Hazard
Affected units
9,287

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • Description: Federarm 3kg
  • 3 polig (Swing)
  • 0376289
  • Federarm 12-18kg
  • 5-polig Kamera eco
  • 0376290
  • Federarm TFT Stop AC 2000
  • 9-15kg
  • 0376291
  • Federarm TFT Stop AC 3000
  • 12-18kg
  • 0376292
  • Federarm TFT Stop Space bis 30kg
  • 0376293
  • Federarm 3-polig NRH
  • 0376294
  • Federarm 5-polig NRH
  • 0376295
  • Federarm 3-polig NRH gerader Abgang
  • 0376296

Distribution

Distributed nationwide across the United States.

The notice also names 1 state specifically:

Part of a larger recall action

This product is one of 5 recalled by Trumpf Medical Systems, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →

Related recalls

Same manufacturer · Trumpf Medical Systems, Inc.

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Same hazard · structural failure

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