Product Wiki · Recalls · U.S. FDA — Device Enforcement

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. — recall Z-2155-2012

U.S. FDA — Device Enforcement · United States · 2012-04-23 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2155-2012
Date of alert: 2012-04-23
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Stryker Spine
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 48250030

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

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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