Stryker Spine: Medical Device Recall in 2012 - (Recall #: Z-2155-2012)

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:

LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the USA by: Stryker Spine. 2 Pearl Ct. Allendale, NJ 07401. Provides access to the thoracic and lumbar spine from a posterior approach via a small incision.

Product Classification:

Class II

Date Initiated: April 23, 2012

Date Posted: August 15, 2012

Recall Number: Z-2155-2012

Event ID: 62648

Reason for Recall:

Stryker received three reports involving blades of the Luxor Retractor becoming disassembled from the base causing the retractor to collapse insitu.

Status: Terminated

Product Quantity: 30 devices

Code Information:

Lot Code: 093309

Distribution Pattern:

Worldwide Distribution -- US, Switzerland, Netherlands, Brazil, Hong Kong, Germany, and Taiwan.

Voluntary or Mandated:

Voluntary: Firm initiated