Featured

Pfizer Recalls Lo/Ovral-28 and Norgestrel / Ethinyl Estradiol Birth Control Medications

norgestrel ethinyl estradiolPfizer Inc. has recalled 14 lots of Lo/Ovral®-28 (norgestrel and ethinyl estradiol) and 14 lots of Norgestrel and Ethinyl Estradiol (generic) birth control pills in the United States (see lot numbers below). Pfizer found that some blister packs may contain an inexact count of inert or active ingredient pills and that the pills may be out of sequence. The cause was identified and corrected immediately, but women who use the recalled birth control may be at a greater risk for unintended pregnancy.

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Medical

Eye Infections, Complications Due to Off-Label Usage of Avastin

By Rachelle Matherne

Avastin - Bevacizumab and Eye InfectionsAccording to an FDA advisory issued August 30, 12 patients have developed serious bacterial infections after using intravitreal injections of bevacizumab (Avastin). Of these 12 patients who developed Streptococcus endophthalmitis, which can lead to blindness and brain damage, at least five have lost all remaining vision in their treated eyes. The incidents occurred in three different clinics in Miami, Los Angeles, and Nashville.

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Food

18th Street Deli Recalls Salad Products for Possible Listeria Contamination

18th street deli saladHamtramck, M.I. company 18th Street Deli Inc. has recalled about 118 lbs. of julienne salad products with turkey, ham and hard-boiled eggs. The salads contain eggs that are the subject of an FDA recall due to contamination with Listeria monocytogenes, according to the USDA.

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Products

Specialized Bicycle Components Expands Recall of Tricross Bicycles Due to Fall Hazard

Bike Forks Specialized Bicycle Components has expanded a recall of their 2012 bikes with Advanced Group carbon forks to include an additional 460 units, bringing the total bikes affected in this Specialized recall to about 14,200.

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Urgent Recalls

Darvocet Recall – Potentially Fatal Heart Abnormalities Final Straw

Darvocets Have Been Recalled - Click here for more information!Xanodyne Pharmaceuticals, Inc. is cooperating with the FDA in recalling Darvocet and Darvon, their versions of the pain killer propoxyphene. Darvon, which is also sold as Darvocet (with acetaminophen added), could cause serious and potentially fatal heart rhythm abnormalities, according to new clinical data reviewed by the FDA.

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Recalled Food, Vehicles, Drugs and Consumer Products:

US Recall News is a non-government, privately-owned website dedicated to bringing you news and information about the latest consumer product recalls, including recalled food, vehicles, pharmaceutical drugs and more.

USRCN endeavors to bring you up-to-date, timely information about recalls and product safety news. Recalled products appear on this website as soon as we are able to publish them. Sometimes this may be a few days or longer from the time the product recall has been officially announce, and sometimes we are made aware of - and publish - recalls before an official announcement has been made.

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Recalled Toys

Toys Distribution Inc. Recalls Rattles Due to Choking Hazard

The recalled rattles can break into small parts, posing a choking hazard to young children and violating the federal safety requirements for rattles. In addition, the size of the handle on some of the rattles is small enough to enter an infant's mouth, lodge in the throat and cause a choking hazard or lead to bruises and lacerations.

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December 14, 2011 | Leave a Comment

Build-A-Bear Recalls 19,720 Teddy Bear Swimwear Sets: Strangulation Hazard

Build-A-Bear Workshop is recalling approximately 19,720 Swimwear Sets with and inflatable inner tube because the inner tube can be a strangulation hazard for small children.

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November 17, 2011 | Leave a Comment

Battat Magnetic Sketchboards Recalled: Magnetic Pen Tip Choking Hazard

About 95,000 Toulouse-LapTrec magnetic sketchboards have been recalled because the tip of the magnetic drawing pen can come loose, which is a choking hazard for children.

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November 3, 2011 | Leave a Comment


Urgent Recalls

FDA Classifies Riata and Riata ST Silicone Defibrillation Leads as Class I Recall

The FDA has classified this recall as a Class I recall because of the potential risk of serious injury or patient death if affected devices malfunction.

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December 16, 2011 | Leave a Comment

Abbott Diabetes Care Recalls Certain Lots of Precision Xtra, Precision Xceed Pro, MediSense Optium, Optium, OptiumEZ and ReliOn Ultima Blood Glucose Test Strips

Abbott Diabetes Care has initiated a recall of 359 lots (approximately 359 million strips) of Precision Xtra, Precision Xceed Pro, MediSense Optium, Optium, OptiumEZ and ReliOn Ultima Blood Glucose Test Strips in the United States and Puerto Rico.

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December 24, 2010 | Leave a Comment

Bassettbaby Recalls to Repair Drop-Side Cribs Due to Entrapment, Suffocation and Fall Hazards

THE RECALLED CRIBS ARE WOOD WITH A METAL MATTRESS SUPPORT AND HAVE A DROP SIDE WITH EXTERNAL PLASTIC HARDWARE. THE CRIBS WERE SOLD IN A VARIETY OF FINISHES. A LABEL IS ATTACHED TO THE FOOTBOARD OR HEADBOARD WITH THE NAMES BASSETTBABY OR BASSETT FURNITURE INDUSTRIES, INC.

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November 23, 2010 | Leave a Comment