The Recall Desk

Manufacturer

Stryker Spine

29 recalls in our database name Stryker Spine as the manufacturing or recalling firm.

What the numbers show

Total
29
Critical
0
Severe
5
Most recent
2025-04-09

Of the 29 recalls from Stryker Spine we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (17%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–29 of 29

  • ModerateFDA (Devices)·Z-2235-2012·2012-08-29

    Stryker Spine Recalls Instructions for Use Due to Sterile Marking Error

    Stryker Spine is recalling 40 units of Instructions For Use for TRIO+ Standard Post Screws because the front cover was incorrectly marked with a 'Sterile' logo.

    Product
    The Instructions For Use for the following: Stryker TRIO+ 4.5 x 45 mm STANDARD POST SCREW Stryker TRIO+ 4.5 x 50 mm STANDARD POST SCREW Stryker TRIO+ 4.5 x 55 mm STANDARD POST SCREW Stryker TRIO+ 5.5 x 45 mm STANDARD POST SCREW Stryker TRIO+ 5.5 x 60 mm STANDARD POST SCREW
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2155-2012·2012-08-15

    Stryker Luxor Retractor Base Recalled Due to Blade Disassembly

    Stryker Spine is recalling 30 Luxor Retractor Base devices because blades may disassemble from the base, causing the retractor to collapse during use.

    Product
    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 sma
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2176-2012·2012-08-15

    Stryker Spine Recalls Reliance AL Implant Blocker Due to Prong Breakage

    Stryker Spine is recalling Reliance AL Implant Blockers because six reports indicated that prongs on the instruments broke during use.

    Product
    Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant Blocker is a reusable instrument, sterilized prior to use. It allows the surgeon to distract the disc space in the lumbar region of the spine using an anterior or anterolateral approach while also allowing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2033-2012·2012-07-25

    Stryker AVS Navigator Trials Recalled for Shaft Failure

    Stryker Spine is recalling AVS Navigator Trials because the shaft may fail at the junction of the trial head.

    Product
    Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Z.1 Marticot-33610-Cestas -France +33 (0) 5.57.97.06.30 http;//www.stryker.com Distributed in the USA by Stryker Spine 2 Pearl Court. Allendale NJ 07401-1677 USA +1-201-780-8000 Cestas France 3
    Category
    Medical Device
    Distribution
    Distributed nationwide