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Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp. Recalls

All product recalls associated with Stryker Howmedica Osteonics Corp..

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Recall Summary

Total Recalls

1000

Past Year

730

Class I (Serious)

175

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 9621–9640 of 11124 recalls

Stryker Howmedica Osteonics Corp.: Secur-Fit MAX Secure-FIT Plus Max Surgical Protocol. Sur...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Accolade System Surgical Technique; Accolade C - Cemented...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: OnmiFit HFx Surgical Protocol 127 degree and 132 degree ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

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Page 482 of 557Next

FDA

Aug 31, 2009

Nationwide

• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: OmniFit Eon 127 degree and 132 degree Surgical Protocol; ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: CuttingEdge Total Hip Instrumentation Surgical Protocol; ...

Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone.

FDAAug 31, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Imaging: Stryker Imaging, Guardian Services Software, Part Number ...

Firm has determined Guardian Services does not contain 100% data backup for 12 OfficePACS Power customers on a daily basis.

FDAAug 31, 2009Nationwide• Stryker Imaging

Beckman Coulter Inc.: Synchron CX Immuno-Protein Cal, part number: 442840, ot...

A recall was initiated because Beckman has confirmed that the standardization of the Immuno Protein Calibrator Set has been re-established to IFCC Reference Preparation for Plasma Proteins, BCR-470 beginning with lot number M901330.

FDAAug 26, 2009Nationwide• Beckman Coulter Inc.

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Tracheal Tube, Cut to Length, Oral, Siliconized, 2...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Polar Preformed Tracheal Tube, South Oral, Murphy ...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Tracheal Tube, Oral/Nasal, Siliconized, 2.5 mm Pro...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Smiths Medical Hythe Hythe, Kent United Kingdom: Portex Uncuffed Paediatric Sized Tracheal Tube, Oral Nasa...

Pediatric Trachel Tube manufactured with internal diameter smaller than indicated in the label may result in inability to remove secretions and cause partial or complete obstruction of the airway

FDAAug 25, 2009Nationwide• Smiths Medical Hythe Hythe, Kent United Kingdom

Stryker Endoscopy: Stryker Infravision Esophageal Kit, Model Numbers 2201805...

The silicone sheath component of the product detaches from the catheter during removal of the e-kit from the body.

FDAAug 20, 2009AL, AR, CA +37 more• Stryker Endoscopy

Stryker Endoscopy: Stryker Titanium Intraline Anchor, Model Numbers 39104000...

Potential breakage -- product may break while inserting it into the bone during surgery. This may prolong surgery, or, if undetected during surgery, result in retained fragments that may cause metal sensitization or immune response, or necessitate further intervention to retrieve the titanium fragments.

FDAAug 20, 2009Nationwide• Stryker Endoscopy

Dust Collection Switches (Woodstock) – fire hazard (2009)

Fire/Burn Risk

The recalled product is a remote dust collector switch, which remotely turns on and off a woodworking dust collector. The product is a black electrical outlet box that comes with two hand-held remote controls. The electrical outlet box has a label that reads "Remote Dust Collector Switch". Both the electrical box and remote controls have "Shop Fox" molded into the plastic on the top side of the product. Model numbers D3038 & D3346 were printed on the carton but not on the remote control unit. The recalled switches measure 4 and 13/16" long by 3 and 7/16" wide.

CPSCAug 18, 2009Nationwide• Woodstock International, of Bellingham, Wash.

Becton Dickinson & Co.: CLAY ADAMS Dynac III Centrifuge, 120V, Model Number 42010...

Medical laboratory centrifuge component may have been assembled incorrectly and cause disabling of the safety feature which prevents customers from opening the centrifuge while it is spinning.

FDAAug 17, 2009PR• Becton Dickinson & Co.

Workshop Sets (Little Tikes) – choking hazard (2009)

Choking Hazard

The oversized, plastic toy nail is about 3 inches long by 1 inch in diameter and comes in red or blue colors. It has a large round head; about 1 ¼ inches below the head is a plastic ridge, slightly smaller than the nail head and about 1 inch in diameter. They were sold with a variety of Little Tikes Children's products. The names, model numbers and UPC code of the products included in this recall are listed below: Model # Name 0914/430B Electronic Project Workshop SOLD FROM MARCH 1994 THROUGH DEC 2003 UPC: 0-50743-00914-3 UPC: 0-57043-52613-8 0920/612237 Little HandiWorker Workhorse SOLD FROM MARCH 1999 THROUGH JUNE 2009 UPC 0-50743-10920-1 UPC 0-50743-61223-7 4146 Home Improvements 2-Sided Workshop SOLD FROM FEBRUARY 2001 THROUGH JANUARY 2009 UPC 0-50743-04146-4 440Z Swirlin' Sawdust Workshop SOLD FROM APRIL 2004 THROUGH NOVEMBER 2008 UPC 0-50743-38540-7 4028 Black Pickup Truck with Tools SOLD FROM MARCH 2000 THROUGH APRIL 2009 UPC 0-50743-04028-3

CPSCAug 13, 2009Nationwide• Little Tikes, of Hudson, Ohio

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: BrainLab Radiotherapy Treatment Planning Software; Cata...

Failure to conduct important safety checks when using the BrainLab radiotherapy treatment planning software in combination with BrainLab conical collimators could result in unintended radiation outside the conical shaped field, which may lead to serious injury of the patient.

FDAAug 12, 2009Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Beckman Coulter Inc.: Synchron Phenobarbital (PHE) Drug Calibrator 1, P/N 46960...

The recall was initiated because Beckman Coulter has confirmed reports of variability in results with the lots of Phenobarbital (PHE) reagent and calibrator.

FDAAug 11, 2009Nationwide• Beckman Coulter Inc.

Beckman Coulter Inc.: Synchron Phenobarbital (PHE) Reagent, P/N 469785, Class...

The recall was initiated because Beckman Coulter has confirmed reports of variability in results with the lots of Phenobarbital (PHE) reagent and calibrator.

FDAAug 11, 2009Nationwide• Beckman Coulter Inc.

Stryker Medical Div. of Stryker Corporation: Stryker Medical wide transport stretcher, Stryker Medical...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation