Trumpf Medical Systems, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2311-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

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.

Product Classification:

Class II

Date Initiated: May 29, 2012

Date Posted: September 12, 2012

Recall Number: Z-2311-2012

Event ID: 62593

Reason for Recall:

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

Status: Terminated

Product Quantity: 402 units

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.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated