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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 20201–20220 of 21319 recalls

Stryker Howmedica Osteonics Corp.: Triathlon Baseplate Impactor Extractor, Orthopedic manual...

Insertion/Removal Difficulties: The Baseplate Impactor/Extractor may not assemble/disassemble easily to the baseplate.

FDAFeb 23, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Teleflex Medical: Sheridan Sher-I-Bronch Left Endobronchial Tube; an Rx, st...

The distal end of the tube may be printed incorrectly, with catalog numbers V5-16037 and 5-16037 stating 'Bronchial - Right' instead of 'Bronchial - Left', and catalog number 5-16137 stating 'Bronchial - Left' instead of 'Bronchial - Right'.

FDAFeb 23, 2005Nationwide• Teleflex Medical

Plus Orthopedics USA: TC-PLUS Solution Femoral Component, model 21028, Femoral ...

Labeling discrepancy.

FDA

1...1009 101010111012 1013...1066

Page 1011 of 1066Next

Feb 22, 2005

• Plus Orthopedics USA

Bicycle Suspension Seat Post (Cannondale) – Structural Weakness (2005)

The recall involves Lee Chi model 1-X bicycle suspension seat posts. The seat post was manufactured by a component manufacturer for Cannondale and installed on various 2005 model year Cannondale brand bicycles. These seat posts have a natural anodized aluminum finish, a 1-X logo is laser etched on the outer tube, and a black, yellow and red instruction booklet with the 1-X logo is attached. Lee Chi is also known as Promax, but the seat posts are not marked with either name. Specific Cannondale bicycle models with affected seat posts are listed in the table below. Model names are printed on the top tube of the bicycle frame. 2005 Cannondale Bicycle Models Adventure 800 Comfort 600 Feminine Adventure 800 Feminine Road Warrior 800 Adventure 600 Sport Road 1000 Adventure 600 Feminine Sport Road 800 Comfort 800 Sport Road 500 Comfort 800 Feminine Touring 2000 Comfort 600

CPSCFeb 18, 2005Nationwide• Cannondale Bicycle Corporation, of Bethel, Conn.

Boston Scientific: Boston Scientific brand Position Acquisition Module (PAM)...

Fire/Burn Risk

The device has the potential for overheating its transformer and has the potential for fire hazard.

FDAFeb 18, 2005Nationwide• Boston Scientific

Smiths Medical ASD, Inc.: Bivona brand Neonatal TTS Tracheostomy Tubes, sterile, pr...

The word PED was printed on the neckflange instead of the word NEO.

FDAFeb 17, 2005GA, IL, IN +4 more• Smiths Medical ASD, Inc.

Philips Medical Systems Sales & Service Region No. America: Easy Access Image Management System with CL.Net.

Failure to update correctly when re-transmitting an image from the modality.

FDAFeb 16, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America

Roche Diagnostics Corp.: Roche ULTIMATE 5 HBA1C test kit for use with MIRA analyze...

The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results.

FDAFeb 15, 2005Nationwide• Roche Diagnostics Corp.

Remington Medical Inc.: Automatic Cutting Needle, Model: NAC-1820B, Size 18 GA x ...

The stylet hub detaches from the stylet needle.

FDAFeb 15, 2005Nationwide• Remington Medical Inc.

Roche Diagnostics Corp.: Roche ULTIMATE 3 HBA1C test kit for use with MIRA analyze...

The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results.

FDAFeb 15, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche COBAS INTEGRA HBA1c Kits for use with COBAS INTEGR...

The product is not uniform across the cassettes of some lots, which will result in an inconsistent bias of patient results.

FDAFeb 15, 2005Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: BioTek brand Automated Microplate Reader; model ELx800, R...

The parameters loaded in the analyzer for the hepatitis C virus do not match those in the package insert, and patient results may be reported out as false positives or false negatives.

FDAFeb 15, 2005Nationwide• Roche Diagnostics Corp.

Boston Scientific: Constellation Advanced Mapping Catheter, Model numbers 80...

The coating on the product's surface can generate debris, which could then move from the heart towards the brain, resulting in Ischemic events.

FDAFeb 14, 2005Nationwide• Boston Scientific

Gas-Electric Heating Units (Trane/American Standard) – performance issue (2005)

Fire/Burn Risk

The recalled units include 2- through 5-ton Trane and American Standard heating and air conditioning packaged units. Affected units are combination gas heat and air conditioning systems installed outdoors only. Gas furnaces installed indoors are not included in this recall. The units have identification plates displaying the model number; serial number; and the year, month and day of manufacture. The plate is located on one end of the unit. The first four digits of all serial numbers indicate the year, fiscal week and day of manufacture. The recall includes: - All units with model numbers beginning with YCP or YCX and having serial numbers beginning with 3383 through 4475; - All units with model number beginning with YCY or YCZ and having serial numbers beginning with 4282 through 4475.

CPSCFeb 11, 2005Nationwide• Trane and American Standard, divisions of American Standard Inc., of Tyler, Texas

Zimmer Orthopaedic Surgical Products: Zimmer Orthopaedic Surgical Products, Disposable Cuff, Du...

The port/tube bond in the affected cuffs may separate during surgery causing the pressure in the cuff to release.

FDAFeb 11, 2005Nationwide• Zimmer Orthopaedic Surgical Products

BISSELL Carpet Cleaner – handle defect (2005)

The recalled upright carpet deep cleaners have an open handgrip, a partially metal handle and come in a variety of colors. The word "BISSELL" is printed on the front of the unit. The recalled carpet cleaners have date codes beginning with 01, 02, 03 or 04 and include the following models: PowerLifter® Plus (model number 1620) PowerSteamer® ClearView® (model numbers 1692, 1692-1, 1692-R) Power Steamer® (model numbers 1685, 1693, 1693-R, 1693-W, 1694, 1694-1, 1694-R) Power Lifter® (model number 1694-3) Rubbermaid X-tra-Lift™ (model 9E00) The date codes and model numbers are printed on a label on the bottom of the unit. Cleaners with the model number and date codes listed above that are marked "Inspected" on or near the label are not included in the recall.

CPSCFeb 11, 2005Nationwide• BISSELL Homecare Inc., of Grand Rapids, Mich.

Philips Medical Systems Sales & Service Region No. America: Tomoscan

Potential for shift of reference lines.

FDAFeb 10, 2005Nationwide• Philips Medical Systems Sales & Service Region No. America

Bicycle Brake Cables (Shimano) – potential failure (2005)

This recall involves aftermarket Shimano 1.6 mm X 1,700 mm brake inner cables for ATB and road racing bicycles. Dual ended brake cables packaged in quantities of ten have a part number of Y80098400/Z80098400. Individual packages have a part number of Y80098110/Z80098110. All single ended brake cables were packaged individually with part number Y80098300/Z80098300. Brake cables installed on mountain, BMX and flat handlebar bicycles are not affected by this recall.

CPSCFeb 10, 2005Nationwide• Shimano American Corp., of Irvine, Calif.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo DR, model 7278 Single Chamber Implantabl...

Medtronic marquis family of ICD and CRT-D devices having batteries manufactured prior to December 2003 that may experience rapid battery depletion due to a specific internal battery short mechanism. Once a short occurs, depletion can take place within a few hours to a few days, after which there is a complete loss of device function.

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo VR, model 7232 Single Chamber Implantabl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment