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 87181–87200 of 92420 results

Sort:

Newest first Oldest first

BioHorizons Implant Systems Inc One Perimeter Park South: The Maestro System 204-503, Straight Permucosal Ext, 5mm ...

The product labeled as a Straight Permucosal Ext, 5mm x 3mm contained a profile abutment for Cement.

FDAJun 3, 2005MI, PA, TX +1 more• BioHorizons Implant Systems Inc One Perimeter Park South

Plus Orthopedics USA: Cancellous Bone Screw, 6.5 x 50 mm, Model 0214807

Screw is mislabeled as a 50 mm screw when in fact it is 45 mm long.

FDAJun 3, 2005ID, TX, VA• Plus Orthopedics USA

Boston Scientific Corp: Boston Scientific brand pull Gastro-dome (percutaneous en...

Two blades may be heat staked onto the stiletto instead of the expected one blade.

FDAJun 2, 2005Nationwide• Boston Scientific Corp

KitchenAid Coffeemakers – Potential Malfunction (2005)

The recalled KitchenAid® coffeemakers are black, white, red, or blue in color. They are manufactured in 10- and 12-cup models. Consumers can determine if they have one of the recalled coffeemakers by identifying the product's model and serial numbers, which are located on a label on the bottom of the coffeemaker. The affected models include: 10 - cup models KCM120OB KCM120WH KCM300OB KCM300WH 12 - cup models KCM200OB KCM200WH KCM400OB KCM400WH KCM400ER KCM400BU The serial numbers of the affected products begin with the letters WCJ, WCK, WCL, WCM, and WCP.

CPSCJun 2, 2005Nationwide

GVP Ceramic Hair Straightening Iron (Generic Value Products) – Fire Risk (2005)

This hair straightening iron has a black housing with golden-colored ceramic heating plates. "Generic Value Products™" is written on the top of the iron and "GVP™" is written in a white circle on the side of the iron. The iron was packaged in a black and white box with the letters GVP™ in large type in the upper left hand front corner. The SKU is 264800, which is written on the packaging.

CPSCJun 2, 2005Nationwide• Generic Value Products, of Omaha, Neb.

Cheftech Signature Grill (CSPS Metal) – safety retrofit (2005)

The grills included in the safety retrofit are Cheftech Signature Series Grill Model#CT001 starting with Serial # 001 and ending with #030. Serial numbers are denoted on the Rating Plate pictured below. Identifying marks include the Rating Plate label on the back. These are 30,000 BTU LP or NG stainless steel grills. The grill has a rotisserie spit and motor. Other model Cheftech gas grills are not included in the recall.

CPSCJun 2, 2005Nationwide• CSPS Metal Co. of Taiwan

Boston Scientific Corp: Boston Scientific brand Standard PEG (percutaneous endos...

Two blades may be heat staked onto the stiletto instead of the expected one blade.

FDAJun 2, 2005Nationwide• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific brand One Step Button (percutaneous end...

Two blades may be heat staked onto the stiletto instead of the expected one blade.

FDAJun 2, 2005Nationwide• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific brand Low Profile PEG (percutaneous en...

Two blades may be heat staked onto the stiletto instead of the expected one blade.

FDAJun 2, 2005Nationwide• Boston Scientific Corp

Exactech, Inc.: The product is a Finned Tibial Tray. Product is labeled ...

Implant was identified incorrectly at the time of manufacture and then laser etched with the incorrect size information.

FDAJun 2, 2005Nationwide• Exactech, Inc.

Becton Dickinson & Company: BD Unopette -- System Tests (Erythrocyte Fragility Test K...

Formulation problems-lower pH of the solutions may increase Red Blood Cell hemolysis

FDAJun 1, 2005Nationwide• Becton Dickinson & Company

ITECH Hockey Goalie Masks – Safety Non-Compliance (2005)

The recalled hockey goalie masks and replacement wires are non-certified models with a cat-eye design and have the word "ITECH" printed on the sides and front of the mask. The ITECH Profile 2100, 1100 and 8.0 goalie masks came in black or white. A label identifying the model and size (medium or large) is affixed to the rear crown of the helmet. In addition, the back of the helmet has a large red triangular warning label. The ITECH RP607 and RP609 replacement wires are black, white and chrome and include a unique side attachment design - they are attached to the helmet/mask by four screws and posts without the use of any additional clips.

CPSCMay 31, 2005Nationwide• Mission-ITECH Hockey, of Kirkland, Quebec, Canada

Plenum Network Cables (Hitachi Cable) – Installation Defect (2005)

The recalled cables typically were installed in data centers and other commercial applications. The part numbers for the recalled cables are 39419-50 (25-pair, category 5e); 30171-100 (50-pair, category 5e); and 30105-50 (25-pair, category 5). Only HCM brand cables with the following lot numbers are affected by this recall: AE589 and A4309 through A5551. The part number and lot number are printed on the jacket of the cables.

CPSCMay 31, 2005Nationwide• Hitachi Cable Manchester (HCM), Inc. of Manchester, N.H.

Home Interiors Fundraising Candle Tin – Safety Concern (2005)

The recall includes 6.5-ounce individually packaged candle tins that are 3¼ inches wide and 2 inches tall with an approximate burn time of 35 hours. The lidded tins are silver with fragrance name labels on the side. Fragrances include Sandalwood, Suede, Mulberry, Seaside Breeze, Hawaiian Delight, Carrot Cake, Fresh Peach, Baked Apple Pie, Vanilla Crème and Lemon Torte.

CPSCMay 31, 2005Nationwide• Home Interiors & Gifts Inc., of Carrollton, Texas

Go!Data Hard Drive Power Adapters – Electrical Hazard (2005)

The recall involves AC power adapters sold with Go!Data 3.5-inch IDE external hard drive enclosures. The AC adapters were sold only with the drive enclosures. "PRiver" or "MoreTec" is written on the enclosures.

CPSCMay 31, 2005Nationwide

Baxter Healthcare Corp. Rt.: Baxter Interlink System Huber Needle Extension Set; a ste...

Some of the product code 2N3709 extension sets with Y-injections sites were placed in packages labeled as product code 2N3703 extension sets which do not have Y-injection sites.

FDAMay 31, 2005AR, FL, NC +2 more• Baxter Healthcare Corp. Rt.

Northwest Medical Physics Equipment Inc: ISOLOC 4.2 Software Part Number NT-NW-425-520. Image gui...

When the ISOLOC (Version 4.2) profile distance unit is set to "centimeter" and the user clicked the "back" button in the digitizer window, the marker and target coordinates in the localization window erroneously display values ten times greater than the correct values.

FDAMay 31, 2005Nationwide• Northwest Medical Physics Equipment Inc

Applied Biotech Inc: Medplus ER Drug Screen Test Model #5800KAB packaged as 25...

The firm has discovered that a number of distributed devices of the Medplus ER Drug Screen Test may be incorrectly assembled which may give incorrect results. The product is an in vitro test for rapid detection of various drugs such as Amphetamines, Barbiturates, Phencyclidine, Cocaine, Methamphetamine, Tricyclic Antidepressants, Morphine, Tetrahydrocannabinol, & Benzodiazepines in human urine.

FDAMay 31, 2005Nationwide• Applied Biotech Inc

B. Braun Medical, Inc.: Locking Tear-Away Sheath Introducer Product Line. ACCUG...

Reports that the tearaway introducer sheaths have cracked hubs/handles and/or improper peeling of the sheath during use.

FDAMay 27, 2005IN• B. Braun Medical, Inc.

BIOMERIEUX, INC.: Bac T/ALERT 3D Combination Module

A Bac T/ALERT 3D system failed to detect a positive sample in a pediatric BAC T/ALERT PF bottle.

FDAMay 27, 2005Nationwide• BIOMERIEUX, INC.

1...4358 435943604361 4362...4621

Page 4360 of 4621Next