Search Results

Found 6,151 results for "cps products"

Medical DeviceUSFDA Devices

Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge 2.0 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

Pride Mobility Products Corp.
FDA DevicesClass II

Brand Name: Quantum rehab Product Name: Q6 Edge 2.0 Model/Catalog Number: Q6 Edge 2.0 Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Aug 12, 2026Pride Mobility Products Corp.
Medical DeviceUSFDA Devices

Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

Pride Mobility Products Corp.
FDA DevicesClass II

Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller

If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.

Aug 12, 2026Pride Mobility Products Corp.
Safety AlertUSRSS Feed

Taylor Fresh Foods Recalls Products Made With Jalapeno Peppers Because of Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Taylor Fresh Foods Recalls Products Made With Jalapeno Peppers Because of Possible Health Risk

Aug 9, 2026
Food & BeverageUSUSDA FSIS

City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination

City Foods, Inc./Bea's Best Corned Beef
USDA FSISPublic Health A...

City Foods, Inc. Recalls Ready-To-Eat Pastrami and Corned Beef Products Due To Possible Listeria Contamination

Product Contamination

Aug 8, 2026City Foods, Inc./Bea's Best Corned Beef
Safety AlertUSRSS Feed

NatureBest Precut & Produce LLC Voluntarily Recalls Products Containing Jalapenos Due to Potential Salmonella Contamination

Unknown Firm
RSS FeedGeneral Alert

NatureBest Precut & Produce LLC Voluntarily Recalls Products Containing Jalapenos Due to Potential Salmonella Contamination

Aug 8, 2026
Food & BeverageUSUSDA FSIS

FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible Salmonella Contamination

Unknown Firm
USDA FSISPublic Health A...

FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Jalapeños That Have Been Recalled Due To Possible Salmonella Contamination

Product Contamination

Aug 8, 2026
Safety AlertUSRSS Feed

Lexunder Inc Recalls Food to Live Brand Green Powder Products Because of Possible Health Risk

Unknown Firm
RSS FeedGeneral Alert

Lexunder Inc Recalls Food to Live Brand Green Powder Products Because of Possible Health Risk

Aug 7, 2026
Food & BeverageUSUSDA FSIS

Corte Argentino USA LLC Recalls Raw Beef Products Imported Without The Benefit Of Import Reinspection

Unknown Firm
USDA FSISClass I

Corte Argentino USA LLC Recalls Raw Beef Products Imported Without The Benefit Of Import Reinspection

Import Violation

Aug 7, 2026
Food & BeverageUKUK FSA

Greencore recalls three pasta products because of possible contamination with Listeria monocytogenes

Greencore
UK FSAPublished

Greencore recalls three pasta products because of possible contamination with Listeria monocytogenes

The possible presence of Listeria monocytogenes in the products listed above. Symptoms caused by Listeria monocytogenes can be similar to flu and include high temperature, muscle ache or pain, chills, feeling or being sick and diarrhoea. However, in rare cases, the infection can be more severe, causing serious complications, such as meningitis.    Some people are more vulnerable to listeria infections, including those over 65 years of age, pregnant women and their unborn babies, babies less than one month old and people with weakened immune systems.   

Aug 7, 2026Greencore
Food & BeverageUSUSDA FSIS

Shan Distribution Network, Inc. Recalls Ineligible Frozen Siluriformes Breaded Fish Fillet and Stick Products Imported from the United Arab Emirates

Unknown Firm
USDA FSISClass I

Shan Distribution Network, Inc. Recalls Ineligible Frozen Siluriformes Breaded Fish Fillet and Stick Products Imported from the United Arab Emirates

Import Violation

Aug 7, 2026
Safety AlertUSCPSC

A2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries

Unknown Firm
A2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries
CPSCGeneral Alert

A2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries

The recalled battery chargers violate the mandatory standard for consumer products containing button cell or coin batteries, because the charger has lithium coin batteries that can be accessed easily by children. In addition, the coin batteries provided with the battery charger are 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.

Aug 6, 2026
Safety AlertUSCPSC

KC Imports and Exports Recalls Mini Laser Pointer Keychains Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

Unknown Firm
KC Imports and Exports Recalls Mini Laser Pointer Keychains Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
CPSCGeneral Alert

KC Imports and Exports Recalls Mini Laser Pointer Keychains Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

The Mini Laser Pointer Keychains violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can be accessed easily by children, posing an ingestion hazard.?Additionally, the packaging and product do not have the warnings required under?Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Aug 6, 2026
Food & BeverageUSUSDA FSIS

Ukrop's Homestyle Foods Recalls Spaghetti and Chicken Products Due to Possible Foreign Matter Contamination

Ukrop's Homestyle Foods
USDA FSISClass I

Ukrop's Homestyle Foods Recalls Spaghetti and Chicken Products Due to Possible Foreign Matter Contamination

Product Contamination

Jul 31, 2026Ukrop's Homestyle Foods
Safety AlertUSCPSC

Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

Unknown Firm
Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries
CPSCGeneral Alert

Golden Link Recalls Fantastic Four Cups and Captain America Popcorn Helmet Containers with LED Lights Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Mandatory Standard for Consumer Products with Button Cell Batteries

The cups and containers violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. In addition, the products do not bear the warning labels required by Reese's Law. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

Jul 30, 2026
Food & BeverageUKUK FSA

Bon Bons Wholesale Ltd recalls various chocolate products because of undeclared milk and soya

Bon Bons Wholesale Ltd
UK FSAPublished

Bon Bons Wholesale Ltd recalls various chocolate products because of undeclared milk and soya

Milk and soya These products contain milk and soya making them a possible health risk for anyone with an allergy or intolerance to milk or milk constituents and/or an allergy to soya.

Jul 25, 2026Bon Bons Wholesale Ltd
PharmaceuticalUSFDA Drugs

Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

Clinere, Carbamide Peroxide, a) 2 bottles of Clinere Carbamide Peroxide (2 x 0.50 mL) 6.5%, 0.5 fl. oz. (15 mL); b) 1 bottle of Clinere Carbamide Peroxide (0,50 fl. oz. (15 mL), Dist. by: Quest Products LLC, Pleasant Prairie, WI 53158, NDC 68229-102-01.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
PharmaceuticalUSFDA Drugs

AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.

Bell Pharmaceuticals, Inc
FDA DrugsClass II

AUDIOLOGIST'S CHOICE, Carbamide Peroxide 6.5%, 0.5 Fl Oz (15 mL) a) Kit - Washer Bulb Included (NDC 59256-001-02); b) 1 bottle (NDC 59256-836-34), Distributed By: Oaktree Products Inc., St. Louis. MO 63005.

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Jul 22, 2026Bell Pharmaceuticals, Inc
Safety AlertUSCPSC

Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading

Wuxi Leclaire Home Products Co., Ltd., of China
Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
CPSCGeneral Alert

Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading

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

Jul 16, 2026Wuxi Leclaire Home Products Co., Ltd., of China
Safety AlertCanadaHealth Canada

Charlevoisienne and Joe Smoked Meat brand meat products recalled due to Listeria monocytogenes

CFIA
Health CanadaClass 1

Charlevoisienne and Joe Smoked Meat brand meat products recalled due to Listeria monocytogenes

Listeria

Jul 10, 2026CFIA
Safety AlertCanadaHealth Canada

The Butcher Barn brand meat products recalled due to undeclared mustard and soy

CFIA
Health CanadaClass 1

The Butcher Barn brand meat products recalled due to undeclared mustard and soy

Mustard - Soy

Jul 9, 2026CFIA
Food & BeverageUSFDA Food

FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT, SOY LECITHIN - AN EMULSIFIER, NATURAL VANILLA FLAVOR), RAISINS, TAPIOCA DEXTRIN, CONFECTIONERS GLAZE. CONTAINS: MILK, SOY PACKED IN A FAICLITY THAT HANDLES PEANUTS, TREE NUTS, WHEAT, SOY, EGG, SESAME, AND MILK PRODUCTS.

Western Mixers Produce & Nuts, Inc.
FDA FoodClass I

FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT, SOY LECITHIN - AN EMULSIFIER, NATURAL VANILLA FLAVOR), RAISINS, TAPIOCA DEXTRIN, CONFECTIONERS GLAZE. CONTAINS: MILK, SOY PACKED IN A FAICLITY THAT HANDLES PEANUTS, TREE NUTS, WHEAT, SOY, EGG, SESAME, AND MILK PRODUCTS.

Undeclared peanuts.

Jul 8, 2026Western Mixers Produce & Nuts, Inc.
Medical DeviceUSFDA Devices

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884522006613 6DCFS 10884522006620 6DFEN 10884522006644 8DCFN 10884522006651 8DCFS 40884522006690 8DFEN 10884522006675 10DCFN 20884522006535 10DCFS 10884522006545 10DFEN 10884522006569 The Shiley Disposable Decannulation Plug (DDCP) is a universal size and fits any size DCFS, DCFN, DFEN tracheostomy tube. The red DDCP snaplock connector is used to occlude the proximal end of the outer cannula on the Shiley Tracheostomy Tubes. Refer to Table 1 for model types. The DDCP blocks airflow through the tube and directs breathing through the mouth and nose. The Shiley Tracheostomy Tube and the accessory products are intended for use in providing tracheal access for airway management.

Covidien LLC
FDA DevicesClass II

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the Covidien Shiley Disposable Decannulation Plug are: Product Number / UDI-DI code 4DCFN 10884522006576 4DCFS 10884522006583 4DFEN 10884522006606 6DCFN 10884522006613 6DCFS 10884522006620 6DFEN 10884522006644 8DCFN 10884522006651 8DCFS 40884522006690 8DFEN 10884522006675 10DCFN 20884522006535 10DCFS 10884522006545 10DFEN 10884522006569 The Shiley Disposable Decannulation Plug (DDCP) is a universal size and fits any size DCFS, DCFN, DFEN tracheostomy tube. The red DDCP snaplock connector is used to occlude the proximal end of the outer cannula on the Shiley Tracheostomy Tubes. Refer to Table 1 for model types. The DDCP blocks airflow through the tube and directs breathing through the mouth and nose. The Shiley Tracheostomy Tube and the accessory products are intended for use in providing tracheal access for airway management.

Due to product labeling incorrectly including the symbol indicating non-DEHP (Bis(2-ethylhexyl) phthalate as the product includes 30 to 35% DEHP.

Jul 8, 2026Covidien LLC
Safety AlertCanadaHealth Canada

TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns

Marketed health products
Health CanadaGeneral Alert

TAVNEOS (avacopan) and Health Canada’s Review of Data Integrity Concerns

New safety information - Product safety

Jul 7, 2026Marketed health products
Safety AlertCanadaHealth Canada

JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)

Drugs and health products
Health CanadaType III

JAMP Chlorthalidone 12.5 mg tablet: Out of specification (Dissolution)

Product quality

Jul 6, 2026Drugs and health products

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.