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Vehicle RecallUSNHTSA

Prevost Car (US) Inc. - Exterior Driver Side Mirror May Detach

Prevost Car (US) Inc.
NHTSAVISIBILITY

Prevost Car (US) Inc. - Exterior Driver Side Mirror May Detach

A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.

Feb 19, 2026Prevost Car (US) Inc.
Food & BeverageUSUSDA FSIS

Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection

Unknown Firm
USDA FSISClass I

Sobico USA LLC Recalls Siluriformes Fish Products Imported Without The Benefit of Import Reinspection

Import Violation

Feb 19, 2026
Condor HMS Triple carabiners
Australia ProductsClimbing and ab...

Condor HMS Triple carabiners

The gate can malfunction and may not close automatically on affected carabiners when used.

Feb 19, 2026
The Cooks Collective Culinary Professional Stand Mixer
Australia ProductsHome electrical...

The Cooks Collective Culinary Professional Stand Mixer

The product can generate or retain electric charge when used. The electric charge level exceeds the limit allowed under Australian electrical standards. As a result, the user can receive an electric shock if they simultaneously touch the beater shaft and the earthed metal enclosure.

Feb 19, 2026
Food & BeverageUSUSDA FSIS

Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination

Ajinomoto Foods North America
USDA FSISClass I

Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination

Product Contamination

Feb 19, 2026Ajinomoto Foods North America
Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
CPSCGeneral Alert

Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails

The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.

Feb 19, 2026Ningbo Shenyu Medical Equipment Co., Ltd., of China
JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
CPSCGeneral Alert

JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries

The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Feb 19, 2026
Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
CPSCGeneral Alert

Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban

The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.

Feb 19, 2026
Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging
CPSCGeneral Alert

Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging

The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Feb 19, 2026
Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
CPSCGeneral Alert

Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear

The recalled sleepwear violates the mandatory flammability standard for children's sleepwear, posing a risk of burn injuries to children.

Feb 19, 2026
Safety AlertCanadaHealth Canada

Monarch Platform

Medical devices
Health CanadaType II

Monarch Platform

Performance

Feb 19, 2026Medical devices
Safety AlertCanadaHealth Canada

BioFlo Dialysis Catheter With Endexo Technology

Medical devices
Health CanadaType II

BioFlo Dialysis Catheter With Endexo Technology

Performance

Feb 19, 2026Medical devices
Safety AlertCanadaHealth Canada

Bipolar Hugo RAS Systems

Medical devices
Health CanadaType II

Bipolar Hugo RAS Systems

Performance

Feb 19, 2026Medical devices
Food & BeverageFranceRappelConso

osito serie oro - kaki persimon osito serie oro espagne cat1 cal 10-12-14-16-18-20 lot 2900

osito serie oro
RappelConsovolontaire (san...

osito serie oro - kaki persimon osito serie oro espagne cat1 cal 10-12-14-16-18-20 lot 2900

dépassement de lmr pour le lambda-cyhalothrine (?+?+s isomères). arfd 268.1%.

Feb 19, 2026osito serie oro
PharmaceuticalUSFDA Drugs

ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)
FDA DrugsClass II

ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.

Presence of Foreign substance - potential presence of metal particulate matter

Feb 18, 2026F.H. INVESTMENTS, Inc. (dba Asteria Health)
Medical DeviceUSFDA Devices

Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD
FDA DevicesClass III

Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor

Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.

Feb 18, 2026SUREPULSE MEDICAL LTD
Food & BeverageUSFDA Food

a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children

KPCM New York Inc.
FDA FoodClass II

a.) Preema brand Bright Red Food Colour Powder; Net Weight .88oz/25gm; packaged in small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children b.) Preema brand Orange Food Colour Powder; Net Weight .88oz/25gm; packaged in a small plastic bottle; INGREDIENTS: SODIUM CHLORIDE, COLOUR (TARTRAZINE, CARMOSINE, ALLURA RED) CHECK THE LEGAL LIMIT, CONTAINS NO ANIMAL MATTER. E102, E122, E129 may have an adverse effect on activity and attention in children

Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40

Feb 18, 2026KPCM New York Inc.
Medical DeviceUSFDA Devices

Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.

Hologic, Inc
FDA DevicesClass II

Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.

Presence of particulates in affected devices that can be deposited into breast tissue during use.

Feb 18, 2026Hologic, Inc
Medical DeviceUSFDA Devices

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

Medline Industries, LP
FDA DevicesClass II

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.

Feb 18, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710FJ282CRH;

Medline Industries, LP
FDA DevicesClass I

Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710FJ282CRH;

These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Feb 18, 2026Medline Industries, LP
Food & BeverageUSFDA Food

Karison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; Distributed By: Karison Foods & Snacks Inc.; 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.

Karison Foods & Snacks, Inc.
FDA FoodClass II

Karison brand ALSI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar Flax Seeds, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00251 2; Distributed By: Karison Foods & Snacks Inc.; 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.

Product contains milk, which is undeclared in the ingredient statement.

Feb 18, 2026Karison Foods & Snacks, Inc.
Medical DeviceUSFDA Devices

Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X

Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.

Feb 18, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B

Medline Industries, LP
FDA DevicesClass II

Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B

Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

Feb 18, 2026Medline Industries, LP
Food & BeverageUSFDA Food

Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.

Karison Foods & Snacks, Inc.
FDA FoodClass II

Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.

Product contains milk, which is undeclared in the ingredient statement.

Feb 18, 2026Karison Foods & Snacks, Inc.
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