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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

731

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 10301–10320 of 11123 recalls

Stryker Howmedica Osteonics Corp.: Duracon Total Knee Modular Femoral Component; Non-Porous ...

Loose fixation pegs: One lot of femoral components may have loose fixation pegs.

FDAOct 17, 2006GA, IN• Stryker Howmedica Osteonics Corp.

Beckman Coulter Inc: FC 500 MPL Flow Cytometry System with MXP Software Versio...

The ratio parameter assignments (numerator and denominator) of a protocol may inadvertently change after the Parameter Selection Dialog box is accessed. Issue limited only to protocols utilizing the Ratio parameter such as LeukoSure and DNA Cell Cycle.

FDAOct 17, 2006Nationwide• Beckman Coulter Inc

Milwaukee Notions, Inc: OneTouchBasic/Profile and OneTouch Ultra- Blood Glucose t...

Counterfeit (manufacturer unknown)

FDAOct 10, 2006

1...514 515516517 518...557

Page 516 of 557Next

Nationwide

• Milwaukee Notions, Inc

BV4000 Blower/Vacs (Black & Decker) – Fire Risk (2006)

Fire/Burn Risk

This recall involves Black & Decker model BV4000 Type 1 blower/vacs. The model and type number are printed on a name plate on the right side of the unit. The blower/vacs have an orange housing and a black blower assembly.

CPSCOct 10, 2006Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand: Fisher & Paykel IW930 CosyCot Infant Radiant Warmer (wit...

This firm has received Product Complaint Reports concerning bending of the pivot plate. The elevator base of the CosyCot Infant Warmer incorporates a pivot plate which forms part of the mechanism allowing the CosyCot to raise and lower in height. A bent pivot plate generally results in the Warmer being unable to elevate properly. Other component failures may result.

FDAOct 9, 2006Nationwide• Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place Auckland New Zealand

Konica Minolta Medical Imaging USA, Inc.: Konica Minolta PrintLink III Model - ID/IV, code no. 07...

The power supply of a unit located in Japan overheated and caused a smoke condition and a small amount of flame coming off the unit.

FDAOct 6, 2006Nationwide• Konica Minolta Medical Imaging USA, Inc.

Stryker Howmedica Osteonics Corp.: Duracon Total Knee Distal Femoral Locking Screw for 5 mm ...

Stryker Orthopaedics became aware that a box labeled as Duracon Total Knee Distal Femoral Locking Screws for 5 mm spacer, may actually contain a 10 mm screw.

FDAOct 5, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Cook Endoscopy: Fusion OMNI ERCP Catheter, Wilson Cook Medical, GI Endosc...

Injection through the flush port of these ERCP catheters may be compromised due to omission of a manufacturing activity.

FDAOct 5, 2006Nationwide• Cook Endoscopy

Dako Colorado, Inc.: Eridan Automated Slide Stainer and Support Cart, REF E300...

Automated slide staining device may not stain speciman slides correctly, and therefore slides cannot be used for patient diagnosis.

FDAOct 2, 2006CA, IN, NC +1 more• Dako Colorado, Inc.

Suave Kids Bath Set (Almar) – Choking Risk (2006)

Choking Hazard

This recall involves "Suave" brand bath sets that contain a 2-in-1 shampoo, bath sponge, and various other toy animal and character bath products. The baths sets are packaged in brightly colored vinyl bags with a clear window. Style numbers involved in this recall are: SVK 9498, 9499, 9501, 9506, 9507 and 9508. The style numbers are located on the back and/or bottom right corner of the package, above the UPC code.

CPSCSep 27, 2006Nationwide• Almar Sales Co., of New York, NY

Stryker Howmedica Osteonics Corp.: Triathlon Total Knee system Primary Tibial Baseplate #5 B...

Stryker Orthopaedics became aware that one lot of the Triathlon Primary Beaded PA Baseplate Size 5 may not have the Peri-Apatite coating.

FDASep 21, 2006AL, GA, OR +3 more• Stryker Howmedica Osteonics Corp.

Cook, Inc.: Cook Zilver 635 Biliary Stent - Expanding Stent, delivery...

The side of the boxes give incorrect sizes for these stents. The label front is correct. (side label-5x40-front label-8x40)

FDASep 21, 2006ID, IN• Cook, Inc.

Candie's Hoodie (Cayre Group) – Strangulation Risk (2006)

The recalled hoodie style zip front hooded sweatshirts were sold in four youth sizes S (7-8), M (9-12), L (14) and XL (16.) The sweatshirts have drawstrings through the hood and were available in two colors, Blue Bell and Demitasse. A tag sewn on the inside of the garment reads "Candie's."

CPSCSep 20, 2006Nationwide• The Cayre Group, of New York, N.Y.

Stryker Howmedica Osteonics Corp.: Triathlon MIS AP Sizer Body - Left and Right; Catalog Nu...

Assembly problems: MIS instruments (Triathlon MIS AP Sizer Body - Left; Triathlon MIS Sizer Body - Right; Triathlon MIS Femoral Adjustment Block and Triathlon MIS Modular Capture) may not assemble properly.

FDASep 19, 2006IL, MI• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Triathlon MIS Modular Capture;Catalog Number: 6541-5-723;...

FDASep 19, 2006IL, MI• Stryker Howmedica Osteonics Corp.

Stryker Howmedica Osteonics Corp.: Triathlon MIS Femoral Adjustment Block;Catalog Number: 65...

FDASep 19, 2006IL, MI• Stryker Howmedica Osteonics Corp.

Beckman Coulter Inc: Coulter LH700 Series Hematology Analyzers, Part Number 66...

There is a potential for erroneous yet credible results for Body Fluids on the LH700 series hematology analyzers when a cassette label fails to read and the subsequent sample is cycled in Body Fluid mode.

FDASep 12, 2006Nationwide• Beckman Coulter Inc

Kendall a Division of Tyco Healthcare Group LP: Kendall Monoject Syringe with Hypodermic Needle, 3cc syri...

Incorrect needle: There is an incorrect needle configuration on the syringe. The correct needle has a 27 gage A-bevel, the needle on the syringe has no bevel, typically used for dental irrigation.

FDASep 11, 2006Nationwide• Kendall a Division of Tyco Healthcare Group LP

Stryker Instruments Div. of Stryker Corporation: Stryker Navigation System, eNlite System with Dell laptop...

Fire/Burn Risk

A component of the device is a Dell laptop computer, which contains batteries that are under recall because they can overheat and cause a fire.

FDASep 8, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation

Stryker Instruments Div. of Stryker Corporation: Stryker Navigation System Remote Planning Stations with D...

Fire/Burn Risk

A component of the device is a Dell laptop computer, which contains batteries that are under recall because they can overheat and cause a fire.

FDASep 8, 2006Nationwide• Stryker Instruments Div. of Stryker Corporation