États-Unis Recalls

Everything Sprouts, LLC Expands Voluntarily Recall to Include Robust Radish Mix Due to Potential E. Coli and Salmonella Risk

Magic Tilt Trailers, Inc. - Weld Failure May Allow Winch to Detach

A detached winch may increase the risk of injury to people near the trailer.

Panorama Produce Recalls Mangoes Due to Possible Salmonella Contamination

Jayco, Inc. - Incorrect GAWR on Certification Label

Referencing the incorrect weight could result in the trailer being overloaded, increasing the risk of a crash.

Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official

The recalled baby toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of children’s throat and become lodged, posing a risk of respiratory distress and deadly choking hazard.

HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards

The glued knot on the elastic cord can become untied on the recalled product, allowing young children access to the small wooden and plastic pieces, posing a risk of serious injury or death from choking and ingestion hazards.

Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers

The recalled walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard.

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter

Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging

The recalled numbing wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging of the wipes is not child-resistant, posing a risk of serious injury or death from poisoning if the contents of the wipes are ingested by young children.

Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators

The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.

Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard

The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children due to an entrapment hazard.

Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled

Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.

AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard

When the amplifiers are used with aftermarket metal base tubes, the bare metal can become electrified, posing a risk of serious injury or death from electrocution.

Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard

The light bars can overheat or produce flames, posing a risk of serious injury from a fire hazard.

Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of injury or death from shock and electrocution hazards.

Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D

The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing a risk of serious injury or death from shock and electrocution hazards.

Altec Industries, Inc. - Strobe Light May Short Circuit

An electrical short-circuit can increase the risk of a fire.

Ana Salazar Modela Tu Cuerpo Inc. Issues Nationwide Voluntary Recall of Lipofit Extreme Fat Burner 2.0 Due to Presence of Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX UPCs 73296608113; 73296600558; 73296610927; 73296600559; 732966107055; 02060042710

Potential Salmonella Javiana contamination

One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device.

Devices could potentially be occluded or partially occluded.

Whole Foods Salsa, Heirloom Tomato. Keep Refrigerated. Packed in various sized clear plastic containers. Product is weighed and a finished product label is applied. Products contain the following PLU Cods located under label bar code: 22860200000, 24091700000, 24118800000, 25024800000, 29648100000, 29648700000, 46000049560. Packed for Whole Foods Market, located at either 1745 W. Market Street, Akron, OH 44313 or 4301 W. William Cannon, Austin, TX 78749.

Salsa and Guacamole products were made with jalapenos that may be contaminated with Salmonella.

Get Fresh Produce Jalapeno Peppers. Item 01896 - 2 lb. box; Item 01894 - 10 lb. box

Potential Salmonella contamination

Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).

The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.

American Contract Systems medical procedure kits and trays labeled as: 1) ANTERIOR CERVICAL PACK - 205988, Model Item Number MHAC65AH; 2) SPINE PACK - 206013, Model Item Number MHSP99AF.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.