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 66861–66880 of 68218 results

Sort:

Newest first Oldest first

Philips Medical Systems Sales & Service Region No. America: BV29 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: BV26 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Merit Medical Systems, Inc: Merit MAK Mini Access Kit, 4 French (1.3mm)

Firm received a report of an introducer sheath separating from its hub while in the patient. Surgery was successful in removal, even though the sheath kept breaking during the attempt.

FDAJul 20, 2004Nationwide• Merit Medical Systems, Inc

Philips Medical Systems Sales & Service Region No. America: BV25 Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: BV 25 Gold Mobile X-Ray System

Potential for c-arm to move due to loose screws

FDAJul 20, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Celsion Corporation: Prolieve Thermodilatation System, model number M006880800...

Software controlling a medical device for patient treatment may malfunction and cause thermal injury to patient.

FDAJul 19, 2004Nationwide• Celsion Corporation

Biosense Webster, Inc.: Stockert 70 Radio Frequency Ablation Generator

Generator Failure resulting increase of catheter temperature that could not be controlled by power reduction.

FDAJul 16, 2004Nationwide• Biosense Webster, Inc.

Boston Scientific Corporation: Express 2 Monorail Coronary Stent Systems (bare metal ste...

Due to characteristics in the delivery catheters that have the potential to impede balloon deflation during a coronary angioplasty procedure.

FDAJul 16, 2004Nationwide• Boston Scientific Corporation

Bock, Otto, Orthopedic Ind, Inc: Modular Knee Joint with Friction Brake

Braking Plates of the 3R90 and 3R92 Modular Knee Joint with Friction Brake may become dislodged which may cause the braking performance of the knee to malfunction.

FDAJul 15, 2004Nationwide• Bock, Otto, Orthopedic Ind, Inc

Diasorin Inc.: DiaSorin GammaCoat Androstenedione - [125I] RIA Kit Catal...

Standards used in the GammaCoat Androstenedione Radioimmunoassay Kit appeared yellowish in color and were gelatinous upon reconstitution.

FDAJul 15, 2004KY, MA, MN• Diasorin Inc.

Cryolife Inc: CryoValve, Pulmonary Valve & Conduit

A pre-implant swab culture of the aortic valve, which was procured from the same donor, was positive for Methicillin resistant Staphyococcus aureus.

FDAJul 15, 2004CA, IN• Cryolife Inc

Stryker Instruments, Instruments Div.: Stryker Navigation System - Hip Module Patient Tracker, g...

The tracker is not locking adequately to the anchoring pin, resulting in unacceptable movement, which will affected the patient tracker system.

FDAJul 14, 2004Nationwide• Stryker Instruments, Instruments Div.

Wright Medical Technology Inc: Guardian Distal Femur Axial Pin

Potential for self -locking axial pin to dislodge and 'back out'.

FDAJul 14, 2004Nationwide• Wright Medical Technology Inc

Roche Diagnostics Corp.: Roche brand Reflotron GOT (AST), 30 test strips; catalog ...

Coating defect may result is falsely decreased patient and/or control results.

FDAJul 14, 2004Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche brand Reflotron GPT (ALT) 30 test strips; catalog #...

Coating defect may result is falsely decreased patient and/or control results.

FDAJul 14, 2004Nationwide• Roche Diagnostics Corp.

Smiths Medical ASD, Inc.: Thermovent 1200, Heat and Moisture Exchanger Catalog # 5...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: ThermovenT 600, Heat and Moisture Exchangers Catalog #...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc.: Portex Thermovent T, Heat and Moisture Exchangers Catalo...

Sterility of the device is compromised due to lack of package integrity

FDAJul 13, 2004Nationwide• Smiths Medical ASD, Inc.

Medikmark, Incorporated: Staple Removal Set/Kit; a sterile Rx convenience kit cont...

The tip of the staple remover may puncture a hole in the wall of the tray, compromising the sterility of the kit.

FDAJul 12, 2004Nationwide• Medikmark, Incorporated

Medex Inc: Disposable Oxygen Mask & Bag, Adult Non-Rebreathing Mask ...

The non-rebreathing masks and watertraps were manufactured with natural rubber or rubber by-products and were not labeled appropriately as containinig latex.

FDAJul 12, 2004CA, CO, FL +8 more• Medex Inc

1...3342 334333443345 3346...3411

Page 3344 of 3411Next