Home / Recalls / Trumpf Medical Systems, Inc. / Z-2311-2012

Z-2311-2012 Class II Terminated

Recalled by Trumpf Medical Systems, Inc. — Charleston, SC

FDA device recall Z-2311-2012 was initiated by Trumpf Medical Systems, Inc. on May 29, 2012 and is designated Class II. Reason for recall: Cracks can arise on the welded seam on the rear joint. The recall status is terminated (terminated Apr 11, 2013). Affected quantity: 402 units.

Recall details

Product Type: Devices
Report Date: Sep 12, 2012
Initiation Date: May 29, 2012
Termination Date: Apr 11, 2013
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 402 units

Product description

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.

Reason for recall

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

Distribution pattern

Worldwide Distribution - USA including CA, OH, OK, NY, PA, TX, WY and the country of Canada

Code information

I.D. on nameplate: FA AC3 or FA AC3000; Material #1920632, Serial #011201602557 to 011201602588; Serial #011203602617 to 011202602621; Serial #011203602676 to 011203602695; Serial #011203602756 to 011203602775; Serial #011203602776 to 011203602795; Serial #011204602798 to 011204602817; Serial #011204602861 to 011204602880; Serial #011204602970 to 011204602989; Serial #011205603032 to 011205603081; Serial #011206603118 to 011206603167; Serial #011206603168 to 011206603217; Serial #011207603303 to 011207603314; Serial #011208603316 to 011205603333; Serial #011208603361 - Serial #011209603431 to 011209603462; Serial #011210603572 to 011210603597 and Material #1851710, Serial #3705776 to 3705777 and Serial #4105778 to 4105781.

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2311-2012
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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