Reported Sep 12, 2012 · Terminated

Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178…

Trumpf Medical Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Trumpf Medical Systems, Inc. · 415 Jessen Ln · Charleston, SC · 29492

Is this the product you have?

  • 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.
Lot codes and dates

16 of 16 products

Products covered by this recall
#BarcodesProduct as published
1FA AC3 or FA AC3000
2011201602557011201602588Material #1920632, Serial #011201602557 to 011201602588
3011203602617011202602621Serial #011203602617 to 011202602621
4011203602676011203602695Serial #011203602676 to 011203602695
5011203602756011203602775Serial #011203602756 to 011203602775
6011203602776011203602795Serial #011203602776 to 011203602795
7011204602798011204602817Serial #011204602798 to 011204602817
8011204602861011204602880Serial #011204602861 to 011204602880
9011204602970011204602989Serial #011204602970 to 011204602989
10011205603032011205603081Serial #011205603032 to 011205603081
11011206603118011206603167Serial #011206603118 to 011206603167
12011206603168011206603217Serial #011206603168 to 011206603217
13011207603303011207603314Serial #011207603303 to 011207603314
14011208603316011205603333Serial #011208603316 to 011205603333
15011208603361011209603431011209603462Serial #011208603361 - Serial #011209603431 to 011209603462
16011210603572011210603597Serial #011210603572 to 011210603597 and Material #1851710, Serial #3705776 to 3705777 and Serial #4105778 to 4105781.
Amount recalled
402 units

Where it was sold

Why it was recalled

Cracks can arise on the welded seam on the rear joint.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 11, 2013 · Data as of Sep 19, 6:13 PM UTC

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