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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

742

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 10541–10560 of 11123 recalls

Stryker Howmedica Osteonics Corp.: Meridian PA Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Meridian ST Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Citation AT Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide

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• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Reliance PF Femoral Stem

The V40 femoral head may not properly engage on the referenced V40 cobal chrome femoral hip stems.

FDAAug 24, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Endoscopy: Biosteon brand HA/PLLA Cross Pin, Model Number 234-500-3...

The medical device is misbranded in that the package is labeled as Biosteon Interference Screw in fact contains Biosteon Cross Pin. This mislabeling could disrupt surgery preparation resulting in surgery delay.

FDAAug 23, 2005OR, VA• Stryker Endoscopy

Stork Craft Toy Boxes (Stork Craft) – Manufacturing Flaw (2005)

The recall includes toy boxes with manufacture date codes between November 2002 and July 2004 and the following model numbers and colors: 01520-331 - white, 01520-334 - cherry, 01520-33C - cognac, 01520-33L - oak, and 01520-33N - natural. The manufacture date codes, model numbers, and colors are located on a label underneath the toy boxes. The toy boxes measure 27 inches long by 18 inches wide and 17 inches high. The boxes are constructed of pine.

CPSCAug 19, 2005Nationwide• Stork Craft Manufacturing Inc., of Richmond, British Columbia, Canada

GeoDeck™ Decking (Kadant Composites) – Material Safety Issue (2005)

Laceration Risk

GeoDeck™ is a composite decking product that looks similar to natural wood and is sold in three colors, including: driftwood, cedar and mahogany. The decking materials were manufactured between April 2002 and October 2003. Each decking and railing component has a manufacturing date stamp (day/month/year) on the cut end, which may still be visible on uninstalled materials.

CPSCAug 19, 2005Nationwide• Kadant Composites Inc., of Bedford, Mass.

Stryker Howmedica Osteonics Corp.: Hoffman II compact Sterile Wrist Kit is used in the stabi...

Stryker Orthopaedics became aware that the pin of the Hoffmann II Compact External Fixation System may jam into the Soft Tissue protector.

FDAAug 17, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: T2 Recon Nail System.

The blister pack containing the Recon 6.5 Lag Screws may become damage during shipment resulting in loss of sterility.

FDAAug 12, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Scorpio Total Knee Cruciate Retaining Femoral Component, ...

The Left Scorpio Total Knee Cruciate Retaining Waffle Femoral Component #7 packaged and labeled as left may contain a Right and vice versa.

FDAAug 11, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Kelty Speedster Jogging Strollers (Kelty) – Frame Safety Concern (2005)

The recalled strollers have an aluminum frame and a cloth seat with a sun canopy. The recalled single seat Speedster Deluxe stroller has model number 20050116 and serial numbers: S2000001D0504 through S2000500D0504 and S2000001D0505 through S2000100D0505. The recalled double seat Speedster Deuce Jogging strollers have model number: 20050216 and serial numbers: S3000001D0504 through S3000300D0504 and S3000001D0505 through S3000075D0505. Each stroller has a tag, located inside the child's seat compartment, which lists the model name and model number. A sticker on the rear frame lists the serial number.

CPSCAug 10, 2005Nationwide• Kelty Division of American Recreation Products Inc., of Boulder Colo.

Beckman Coulter Inc: Aqueduct Hematology Workflow Manager, software

Potentail for misidentification of historical patient results within the Aqueduct Hematology Workflow Manager software. In instances where the workflow manager software receives the same patient identifier for more than one patient the Aqueduct Workflow Manager software merges all results into one Patient File. The may cause test results to be associated with the wrong patient.

FDAAug 10, 2005AK, AZ, CA +15 more• Beckman Coulter Inc

Depuy Mitek, a Johnson & Johnson Co.: DePuy Mitek Straightshot Ligament Graft Passer/Protector,...

Mislabeled: The kit contained the incorrect Ligament Passer. The package contained a 9.5 mm instead of the labeled 11.5mm ligament passer

FDAAug 9, 2005CA, NC, VA• Depuy Mitek, a Johnson & Johnson Co.

Trek Diagnostic Systems: VersaTREK Myco AS.

Invitro diagnostic test kit used for testing to confirm the presence of tuberculosis contains interfering bioburden which can cause false positive results.

FDAAug 8, 2005AL, IL, IN +6 more• Trek Diagnostic Systems

Stryker Howmedica Osteonics Corp.: Reamer T-Handle; Non- Sterile; Howmedica Osteonics Corp.,...

Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.

FDAAug 8, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Navigation Reamer T-handle; Non Sterile; Howmedica Osteon...

Stryker Orthopaedics learned that the T-handles have the potential to not engage and not attach to the reamer properly.

FDAAug 8, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Stryker Instruments Div. of Stryker Corporation: Stryker brand Consolidated Operating Room Equipment (CORE...

Potential electrical shock hazard, in that the potential exists for the patient to be exposed to an earth-referenced electrical current.

FDAAug 5, 2005VA• Stryker Instruments Div. of Stryker Corporation

Skytron, Div. The KMW Group, Inc: Skytron General Purpose Surgical Table; Model 6600, Dist....

The release levers can inadvertently release under load while the leg section is positioned at a ninety degree angle causing the leg section to drop.

FDAAug 4, 2005Nationwide• Skytron, Div. The KMW Group, Inc

Cook Urological, Inc.: Cook brand Fascial Dilator; 10FR/37cm, sterile, Rx Only, ...

Mislabeled as to size.

FDAAug 1, 2005CA, FL• Cook Urological, Inc.

Becton Dickinson & Co.: Oxacillin Screen Agar, Catalog 221952, in disposable plas...

Microbiological media for antibiotic susceptibility testing gives false test results.

FDAJul 28, 2005Nationwide• Becton Dickinson & Co.