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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

1000

Class I (Serious)

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 17361–17380 of 21320 recalls

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 6MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

FDAApr 16, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Radiometer America Inc: Waste bottles Part Numbers/Article Numbers: 905-590/D512 ...

When removing the waste bottle from the analyzer waste material may leak both from the analyzer and from the waste bottle.

FDAApr 16, 2009Nationwide• Radiometer America Inc

Stryker Howmedica Osteonics Corp.: Offset Adaptor Trial - 8MM, Triathlon Revision Instrument...

Triathlon Offset Adaptors may seize during surgery and the OR staff may be unable to disassemble the instrument using the removal tool.

1...867 868869870 871...1066

Page 869 of 1066Next

FDA

Apr 16, 2009

Nationwide

• Stryker Howmedica Osteonics Corp.

Merit Medical Systems, Inc.: 8F Prelude Short Sheath Introducer, 4CM in Length with Ma...

External tubing may separate during use, allowing blood loss.

FDAApr 14, 2009CA, CO, GA +4 more• Merit Medical Systems, Inc.

Merit Medical Systems, Inc.: Prelude Short Sheath Introducer, Carolina Kidney and Endo...

External tubing may separate during use, allowing blood loss.

FDAApr 14, 2009CA, CO, GA +4 more• Merit Medical Systems, Inc.

Ascension Orthopedics, Inc: Normed TX 8 Driver, Non-Cannulated (used with the Ascensi...

Screwdriver used with the Ascension Total Foot System not manufactured to specification, resulting in the driver not properly engaging and/or stripping the screws making it difficult to properly seat the screws during surgery.

FDAApr 14, 2009Nationwide• Ascension Orthopedics, Inc

Merit Medical Systems, Inc.: 5F Prelude Short Sheath Introducer, 4CM in Length with Ma...

External tubing may separate during use, allowing blood loss.

FDAApr 14, 2009CA, CO, GA +4 more• Merit Medical Systems, Inc.

Trilliant Surgical LTD: 2.0/2.4 Cannulated Screw Driver Bit, part #210-24-003

Firm received several complaints of field failures, e.g., "broke during surgery" and the firm initiated a design change. A communication to sales staff 04/14/2009 instructed them to recover and reconcile these products from user physicians.

FDAApr 14, 2009CA, GA, IA +12 more• Trilliant Surgical LTD

Hitachi Medical Systems America Inc: Hitachi ECLOS Computed Tomography (CT) Scanners, Software...

Incorrect scale on image: A software error can occur if two (2) different Field-of-View (FOV) settings are registered in a protocol using Multi-Reconstruction. This could cause the image generated to be displayed with the wrong scale factor rendering anatomical measurements incorrect.

FDAApr 14, 2009Nationwide• Hitachi Medical Systems America Inc

Merit Medical Systems, Inc.: 6F Prelude Short Sheath Introducer, 4CM in Length with Ma...

External tubing may separate during use, allowing blood loss.

FDAApr 14, 2009CA, CO, GA +4 more• Merit Medical Systems, Inc.

Hitachi Medical Systems America Inc: Hitachi CXR4 Computed Tomography (CT) Scanners, Software ...

FDAApr 14, 2009Nationwide• Hitachi Medical Systems America Inc

Merit Medical Systems, Inc.: 7F Prelude Short Sheath Introducer, 4CM in Length with Ma...

External tubing may separate during use, allowing blood loss.

FDAApr 14, 2009CA, CO, GA +4 more• Merit Medical Systems, Inc.

Aspen Surgical Products, Inc.: Surgidyne S-Vac round fluted channel silicone drain, 1/8"...

An adaptor, which may be required when connecting the drain to an external device, was not included in the package.

FDAApr 13, 2009Nationwide• Aspen Surgical Products, Inc.

Siemens Medical Solutions USA, Inc: ARTISTE MV Systems (Part Number 8139789), equipped with a...

Unexpected treatment plan alteration-- Software issue may result in unintended modifications to treatment

FDAApr 9, 2009FL, MA, MI +5 more• Siemens Medical Solutions USA, Inc

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals: AccuSure, U-100 31 Gauge, 1cc Insulin Syringe, 5/16" (8mm...

Needles separate from the barrel of the syringes.

FDAApr 9, 2009Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Marina Medical Instruments Inc.: VIPA Veronikis Intra-Fiberoptic Pelvic Assistant, Set Cat...

Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation.

FDAApr 9, 2009Nationwide• Marina Medical Instruments Inc.

Laborie Medical Technologies Cor: Laborie Medical Technologies Urodynamic Catheters, Twin ...

Laborie Medical Technologies reports that there was a mix up in the labeling and packaging of their Urodynamic Catheters. There were 8Fr catheters mixed inside the 6Fr catheter packages.

FDAApr 9, 2009Nationwide• Laborie Medical Technologies Cor

Marina Medical Instruments Inc.: VVD Veronikis Vaginal Dilator - Complete Set Catalog No. ...

FDAApr 9, 2009Nationwide• Marina Medical Instruments Inc.

Marina Medical Instruments Inc.: VNVD Veronikis Neo Vaginal Dilator - Complete Set Catalog...

Marina Medical, Sunrise, FL initiated recall of 46 products of 350 series devices and 47 products of 270 series products because the material used to manufacture the products was not proven to be biocompatible, resulting in risk of temporary skin or tissue irritation.

FDAApr 9, 2009Nationwide• Marina Medical Instruments Inc.

Picis Inc.: PICIS, CareSuite Family- OR Manager (4235), Preop Manager...

Demographic data, most notably allergy and precaution data, can be overwritten with incomplete data or blanks by the interface between non-Picis clinical systems (your "HIS" or "CIS") and certain Picis applications, if that interface is not configured properly.

FDAApr 8, 2009Nationwide• Picis Inc.