Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Depuy Orthopaedics, Inc.

Depuy Orthopaedics, Inc. Recalls

All product recalls associated with Depuy Orthopaedics, Inc..

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 31901–31920 of 37665 recalls

Depuy Orthopaedics, Inc.: DePuy P.F.C. Sigma Knee System, Non-Porous Cruciate Retai...

There may be a crack on the lateral side of the condyle in the posterior chamfer region. The device is used as a Orthopedic knee implant.

FDAMay 7, 2009Nationwide• Depuy Orthopaedics, Inc.

Off-Road Motorcycles (KTM) – Front Fork Failure (2009)

This recall involves model year 2009 KTM off-road motorcycles. The model name and KTM™ logo are located on the right and left shrouds. The following models are included in this recall:Model Name Description 125SX Orange / Black 150SX Orange / Black 250XC-W Orange / Black 300XC-W Orange / Black

CPSCMay 7, 2009Nationwide• KTM North America Inc., of Amherst, Ohio

Smith & Nephew, Inc. Endoscopy Division: Smith & Nephew Endoscopic Disposable Blades: FULL RADIUS ...

Product sterility is compromised due to breach in the sterile packaging.

1...1594 159515961597 1598...1884

Page 1596 of 1884Next

FDA

May 7, 2009

Nationwide

• Smith & Nephew, Inc. Endoscopy Division

Upright Freezers (Fricon) – Fire Hazard (2009)

Fire/Burn Risk

This recall involves the Fricon commercial one-door upright freezers with model number VCV1V. These freezers are typically used in grocery stores and other commercial settings. The model number is found either on a label located in the upper, right corner on the back of the unit or on a label located inside the unit on the lower left side.

CPSCMay 7, 2009Nationwide• Frigocon - Indústria de Frio e Congelação S.A., of Portugal

Beckman Coulter Inc.: UniCel DxC 880i, 860i,680i and 660i Synchron Access Clini...

The recall was initiated after Beckman Coulter confirmed reports of inaccurate Access Intrinsic Factor Ab test results displayed on, or printed from, the UniCel Dxl portion of an integrated workstation listed above. The problem is limited to numerical Intrinsic Factor Ab results produced on integrated systems running UniCel Dxl system software version 4.0, 4.1, or 4.2. The DxC portion of your inte

FDAMay 7, 2009Nationwide• Beckman Coulter Inc.

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: Peripheral Dilatation Catheter, Viatrac 14 Plus 5.0mm x 1...

Abbott Vascular is initiating a recall on the Viatrac 14 Plus 5.0x15 mm Peripheral Dilation Catheter due to a mistake in labeling/packaging.

FDAMay 6, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Abbott Vascular-Cardiac Therapies dba Guidant Corporation: Abbott Vascular, StarClose Vascular Closure System Part N...

Potential sterility issue. Internal component quarantined for possible contamination, was released for sale after going through sterilization procedure.

FDAMay 6, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Philips Healthcare Inc.: Philips IntelliVue Clinical Information Portfolio Softwar...

Error in therapy scheduling: If scheduled orders are documented and edited prior to the orders' original schedule time, ICIP can create a second instance of the same order marked as pending. A second instance of an order may result in a patient receiving duplicate therapy or patients may not receive their scheduled therapies.

FDAMay 5, 2009Nationwide• Philips Healthcare Inc.

Boston Scientific Corp: Boston Scientific EndoVive 24F (8 mm) Safety PEG Kit, Pus...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDAMay 5, 2009Nationwide• Boston Scientific Corp

Philips Healthcare Inc.: CareVue Chart Release C.O Part Number: 862246 Intended f...

Software: A software defect under certain circumstances could lead to the unintended administration of a duplicate dose of a scheduled medication within a single 24 hour period

FDAMay 5, 2009CA, FL, MA +5 more• Philips Healthcare Inc.

Erwin and Poseidon Beanie Hats (Ambler Mountain Works) – Choking Hazard (2009)

Choking Hazard

The Erwin Beanie is primarily green and white yarn knitted to configure a frog with white eyeballs and a red smile. The Poseidon Beanie comes in several colors of yarn and has hand sewn turtles, whales and octopus attached to the beanie. The beanies have the firm's logos "Ambler" or "A" printed on a fabric tag.

CPSCMay 5, 2009Nationwide• Ambler Mountain Works, of Canmore, Alberta, Canada

Stelkast Co: Stelkast Unicondylar Knee Femoral Component SC2462-1. Us...

incorrect size markings on component

FDAMay 5, 2009Nationwide• Stelkast Co

International Technidyne Corp.: Hemochron Jr. ACT- LR Assay (JACT- LR); ITC Catalogue/Cod...

One lot of ACT-LR was released when one finished good testing criteria acceptance limit did not meet acceptance criteria.

FDAMay 5, 2009Nationwide• International Technidyne Corp.

Boston Scientific Corp: Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, P...

The user may be unable to pass the device over the guidewire for placement in the patient, resulting in an inability to use the device.

FDAMay 5, 2009Nationwide• Boston Scientific Corp

GE Medical Systems, LLC: GE Healthcare, CT Perfusion 4 on Advantage Workstation, C...

GE Healthcare has recently become aware of the need to adjust default settings associated with the use of CT Perfusion 4 on the Advantage Workstation, ST and PET/CT consoles that may impact patient safety. The default parameter settings in CT Perfusion 4 may not be optimal in the case of data acquired with longer time sampling intervals such as axial scans with inter scan delay (ISD) greater th

FDAMay 4, 2009AZ, CA, CT +17 more• GE Medical Systems, LLC

Ansell Healthcare Products LLC: Ansell, Derma Prene Ultra, Powder-Free, Smooth Surgical G...

Premature degradation which could result in tearing during use.

FDAMay 1, 2009Nationwide• Ansell Healthcare Products LLC

NRT Nordisk Rontgen Teknik A/S Birkegaardsvej 16 Hasselager Denmark: Celex/GE Precision MPi, REF no.: 02980000 Is an all-digi...

The GE Precision MPi is in violation with 21 CFR Part 1020.32 requiring a signal audible to the fluoroscopist to sound for each passage of 5 minutes of fluoroscopic irradiation time during an examination or procedure.

FDAMay 1, 2009Nationwide• NRT Nordisk Rontgen Teknik A/S Birkegaardsvej 16 Hasselager Denmark

GE Medical Systems, LLC: HiSpeed X/i Computed Tomography operator consoles with th...

It was discovered that the operator console did not have a label affixed in accordance with 21CFR 1010.2 indicating certification to applicable performance standards.

FDAMay 1, 2009AL, CA, CT +9 more• GE Medical Systems, LLC

Philips Medical Systems North America Co. Phillips: The product's marketing brochure states: "1.5T coils and ...

Fire/Burn Risk

Combined use of the Synergy Flex-M / Shoulder Coil 1.5T increases the chance of RF interaction and heating up of the coil. This may result in possible burns of the patient.

FDAMay 1, 2009Nationwide• Philips Medical Systems North America Co. Phillips

Stryker Spine: Stryker Mantis Rod Inserter; Non Sterile, Manufactured by...

The Mantis Rod Inserter Shaft was found to have deformation of the stainless stell split sphere when subjected to high forces, prohibiting the user from being able to grip the rod implantation and the split sphere may separate and fall into the patient.

FDAApr 30, 2009Nationwide• Stryker Spine