Skip to main content

Is My Product Recalled?

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Scan How It Works Saved Get Alerts

Menu

Search All Recalls Latest Recalls Scan Barcode Get Alerts

Categories

Food Recalls Medication Recalls Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Resources

How Recalls Work FAQ Recall Classifications Statistics & Trends About

Your Recalls

Loading...

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 ↗

Search Product Recalls

Try:····

Filters

Category

All Categories Food Medication Baby Products Pet Products Toys Electronics Household Vehicles Medical Devices Other

Time Period

All Time Last 30 Days Last 90 Days Last Year

State

Severity

All Severities Class I (High Risk)Class II (Moderate)Class III (Low)

Source

All Sources FDA CPSC USDA NHTSA

Status

Include terminated recalls

Clear all filters

Showing 65761–65780 of 68218 results

Sort:

Newest first Oldest first

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• Stryker Howmedica Osteonics Corp.

Hamilton Co: Y-valve and T-valve, PSD/4 Syringe Drive Module parts.

The product valve has a high probability of deforming and may result in leakage during use.

FDAAug 24, 2005CA, IN, MA +2 more• Hamilton Co

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

Zimmer Inc.: Zimmer brand Bigliani/Flatow Total Shoulder trabecular me...

The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement.

FDAAug 23, 2005Nationwide• Zimmer Inc.

St. Jude Medical Daig Division: Angio-Seal Vascular Closure Device. Ref 610109. 6F STS ...

Mispackaging-Some Angio-Seal 6F STS Vascular Closure Devices from Lot no. 1146548 have been incorrectly packaged with a 0.035' guidewire instead of a 0.032' guidewire.

FDAAug 22, 2005Nationwide• St. Jude Medical Daig Division

BIOMERIEUX, INC.: VeriCal Calibrator Set

The product is being recalled due to mis-assignment of ISI values associated with VeriCal use.

FDAAug 19, 2005Nationwide• BIOMERIEUX, INC.

GE Medical Systems, LLC: GE Signa Advantage nuclear magnetic resonance imaging sys...

During use of GE Signa nuclear magnetic resonance imaging system, a flexible Teflon tube that was part of the magnet vent system ruptured and allowed the magnet to vent into the scan room. Because of helium pressure inside the room, the scan room door could not be reopened after the patient was removed from the scan room.

FDAAug 19, 2005Nationwide• GE Medical Systems, LLC

Datascope Corp: Panorama Patient Monitoring Network, Cardiac Arrhythmia M...

The software version contains an anomaly which could freeze the unit when the right click button is used on the mouse.

FDAAug 19, 2005Nationwide• Datascope Corp

Tosoh Bioscience, Inc.: Tosoh brand Glycohemoglobin A1c Controls I & II, Catalog ...

The firm has received reports that vials of the Level II were exhibiting poor and inconsistent chromatogram quality thus affecting control results.

FDAAug 18, 2005PR• Tosoh Bioscience, Inc.

Philips Medical Systems (Cleveland) Inc: Gemini GXL PET/CT Systems, 6, 10, 16 slice configurations...

The image balance center point correction algorithm used in CT image reconstruction may cause a disapperance or alteration of small circular anatomical structures that are both near the image center and perpendicular to the image plane. This artifact may lead to the misinterpretation of anatomy at the center of the image.

FDAAug 18, 2005IN• Philips Medical Systems (Cleveland) Inc

C.R. Bard, Inc., Urological Division: Bard * Davol Reliavac 400 Closed Wound Suction Kit * Ster...

An incorrect Y-connector was placed in the kit.

FDAAug 17, 2005AL, CA, FL +6 more• C.R. Bard, Inc., Urological Division

Baxter Healthcare Corp. Rt.: Epidural Infusion Pumps sold under the following labels; ...

Potential overinfusion in the Auto-Ramp mode with software versions 3.00 or higher

FDAAug 17, 2005Nationwide• Baxter Healthcare Corp. Rt.

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.

Unknown Manufacturer: Amplatz Goose Neck Microsnare Kit, Model SK400 (175 cm l...

ev3 has determined that one test unit from each of two lots did not meet mininum tensile strength requirements and therefore the entire lots are being recalled.

FDAAug 16, 2005AL, AR, CA +11 more

International Biophysics Corp: IBC Suction Handle (Sterile), a component of Blood Recove...

Tyvek pouches containing device labeled as sterile have defective seals.

FDAAug 16, 2005FL, IN• International Biophysics Corp

Gambro Renal Products: Prisma continuous renal replacement system.

Critically ill patients undergoing continuous renal replacement therapy may suffer excessive fluid loss.

FDAAug 16, 2005Nationwide• Gambro Renal Products

Siemens Medical Solutions USA, Inc: Magnetom Espree. Magnetic Resonance Imaging System. model...

there is a misalignment of the patient table that may occur between the patient table and the opening to the magnet bore

FDAAug 12, 2005Nationwide• Siemens Medical Solutions USA, Inc

Event Medical: INSPIRATION Ventilator Model Numbers: F7100000-XX, F7200...

Firm received reports of combustion within the blender system of the Inspiration Ventilator.

FDAAug 12, 2005Nationwide• Event Medical

1...3287 328832893290 3291...3411

Page 3289 of 3411Next