Home

US Recall News Covers it All

US Recall News combines all of the news coming out of various government and non-government organizations responsible for disseminating news about different types of recalls in the United States.

We are not associated with any government organization and are an independently owned media outlet. You can learn more about us here.

The easiest way to find what you’re looking for is to search for a product name or model number. We do not claim to have 100% of the recalls you could find in government databases so it’s always a good idea to check there if you don’t see it here. Our terms & privacy policy page explains more. To find out which government agency is responsible for which types of product recalls, along with links to pages where you can report “adverse events”, click here.

Subscribe to our feed by email if you’d like to stay informed about the latest recalled products. You can unsubscribe at any time.

US Recall News » Urgent Recalls

Your one-stop-shop for information on recalled consumer products, pharmaceutical drugs alerts, health supplements recalls, recalled vehicles, automotive parts, boats and more.

After a new study linked Depakote and other valproate medications taken during pregnancy to an increased risk of autism and autism spectrum disorders, the FDA has decided to put its strongest warning for pregnancy associated ... Read more...
Author: Candelaria
Posted: May 15, 2013, 1:01 am
The FDA has warned consumers not to take any dietary supplement containing the ingredient DMAA (dimethylamylamine, which goes by other names as well, listed below), which has been associated with numerous risks, including seizures, heart ... Read more...
Author: Candelaria
Posted: April 30, 2013, 12:41 am
ADM Alliance Nutrition, Inc. (“Alliance Nutrition”) is recalling 50-pound bags of MoorMan’s® ShowTec® 18 Elite Lamb DC, product number 80939MPS, because the product has high levels of copper. There are three lot numbers involved in ... Read more...
Author: The FDA
Posted: January 8, 2013, 12:43 am
About 97,000 Eddie Bauer Rocking Wood Bassinets are being recalled because the bottom locking mechanism can fail to lock properly if a spring is not installed, allowing the bassinet to tip to one side posing a suffocation hazard to infants.
Author: The CPSC
Posted: October 26, 2012, 3:55 pm
The easiest way to keep track of the peanut butter recalls is to bookmark this page, which will automatically update whenever we publish a new recall with the phrase 'peanut butter' in it.
Author: E. Sizemore
Posted: October 16, 2012, 12:47 am
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.
Author: The FDA
Posted: December 16, 2011, 12:00 am
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.
Author: The FDA
Posted: December 24, 2010, 12:00 am
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.
Author: The CPSC
Posted: November 23, 2010, 12:00 am
Xanodyne Pharmaceuticals, Inc. is cooperating with the FDA in recalling Darvocet and Darvon, their versions of the pain killer propoxyphene. Darvocet could cause serious and potentially fatal heart rhythm abnormalities, says the FDA.
Author: E. Sizemore
Posted: November 20, 2010, 1:55 am
12 REPORTS OF INFANTS BETWEEN THE AGES OF 1 MONTH AND 4 FOUR MONTHS WHO DIED WHEN THEY SUFFOCATED IN SLEEP POSITIONERS OR BECAME TRAPPED AND SUFFOCATED BETWEEN A SLEEP POSITIONER AND THE SIDE OF A CRIB OR BASSINET.
Author: The CPSC
Posted: September 20, 2010, 12:00 am
Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter.
Author: The FDA
Posted: August 25, 2010, 12:00 am
THE BOY WAS FOUND HANGING WITH HIS NECK ENTRAPPED BETWEEN THE PLAYARD FRAME AND THE METAL BASE ROD OF THE TENT THAT HAD BEEN PARTIALLY TIED BY PIECES OF NYLON ROPE AND PARTIALLY ATTACHED BY CLIPS. THE TENT WAS TIED TO THE PLAYARD BECAUSE THE CHILD WAS ABLE TO POP OFF THE CLIPS.
Author: The CPSC
Posted: July 16, 2010, 12:00 am
THE ORAL INFLATOR BUTTON IS NOT PROPERLY BONDED TO THE ORAL STEM AND CAN FALL OFF DURING USE, POSING A LEAK OF THE BUOYANCY COMPENSATOR CONTENTS. THIS POSES A DROWNING HAZARD.
Author: The CPSC
Posted: July 1, 2010, 12:00 am
CONSUMERS SHOULD IMMEDIATELY STOP USING THE RECALLED SLINGS AND CONTACT SPROUT STUFF TO RETURN THE SLING FOR A FULL REFUND.
Author: The CPSC
Posted: June 3, 2010, 12:00 am
CPSC HAS RECEIVED TWO REPORTS OF INJURIES THAT OCCURRED WHEN THE STORAGE TRUNKS’ LIDS SUDDENLY CLOSED ON CHILDREN, INCLUDING ONE REPORT OF AN 18-MONTH-OLD GIRL WHO REPORTEDLY SUFFERED BRAIN DAMAGE WHEN THE TRUNK’S LID CAME DOWN ON THE BACK OF HER NECK AND PINNED HER THROAT AGAINST THE RIM OF THE TRUNK.
Author: The CPSC
Posted: May 21, 2010, 12:00 am
AS PART OF ITS COMMITMENT TO ENSURE SAFE SLEEP FOR YOUNG CHILDREN, THE U.S. CONSUMER PRODUCT SAFETY COMMISSION (CPSC) IS ONCE AGAIN WARNING PARENTS AND CAREGIVERS ABOUT DEADLY HAZARDS WITH DROP-SIDE CRIBS.
Author: The CPSC
Posted: May 8, 2010, 12:00 am
STRANGULATIONS IN ROMAN SHADES OCCUR WHEN A CHILD PLACES HIS/HER NECK BETWEEN THE EXPOSED INNER CORD AND THE FABRIC ON THE BACK SIDE OF THE BLIND OR WHEN A CHILD PULLS THE CORD OUT AND WRAPS IT AROUND HIS/HER NECK.
Author: The CPSC
Posted: December 17, 2009, 12:00 am
This device is a vertebral body replacement device that is used in the T1-L5 portion of the spine to replace a collapsed, damaged, or unstable vertebral body due to a tumor or trauma.
Author: The FDA
Posted: November 13, 2009, 12:00 am
The device blocks off the aorta, monitors aortic pressure, and delivers solution to stop the heart during cardiopulmonary bypass procedures.
Author: The FDA
Posted: November 10, 2009, 12:00 am
Penumbra voluntarily conducted a field removal of the devices after learning about the devices potential to kink or ovalize. FDA has been apprised of this action.
Author: The FDA
Posted: October 1, 2009, 12:00 am