Recalls in Illinois (page 18)
4177 recalls.
- Winco Fireworks International Recalls Unity 7 Shot 200 Gram Aerial Cake Fireworks Due to Risk of Serious Injury from Explosion and Burn Hazards
Consumer productReported July 3, 2026 · The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards. - Conair Recalls Over One Million Cuisinart Grill Brushes Due to Ingestion Hazard
Consumer productReported July 3, 2026 · 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... - Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries; Sold on Amazon by JSNJ_Tech Store
Consumer productReported July 3, 2026 · The lithium coin batteries are not sold in child-resistant packaging and do not bear the warning labels as required under Reese's Law. When button cell or coin... - Cooper Lighting Recalls Metalux Optimized High Bay LED Light Fixtures Due to Fire Hazard
Consumer productReported July 3, 2026 · The LED's board can overheat or come into contact with the lens or nearby combustible materials, posing a fire hazard. - Target Recalls Gigglescape™ Under the Sea Popping Toy Due to Choking Hazard
Consumer productReported July 3, 2026 · The clear plastic dome can detach from the blue plastic base, making the small plastic balls inside the toy accessible to children, posing a choking hazard. - AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions; Sold on Amazon by Pretty-Life
Consumer productReported July 3, 2026 · The recalled nursing pillows advertised for infant feeding and tummy time violate the mandatory safety standards for nursing pillows and infant support... - Rowenta Recalls Cordless Vacuum Cleaners Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported July 3, 2026 · The recalled lithium-ion battery in the vacuum cleaner can overheat and ignite, posing a risk of serious injury from fire and burn hazards. - Projecting LED Finger Light Toys Recalled Due to Risk of Serious Injury Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by POPOOO
Consumer productReported July 3, 2026 · The recalled LED finger lights violate the mandatory safety standard for toys because they contain button cell batteries that can be easily accessed by... - Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Consumer productReported July 3, 2026 · The recalled medicated wipes contain lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The packaging... - Topyond Pool Drain Ports with Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold by Jialyduu
Consumer productReported July 3, 2026 · The recalled drain ports with covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly... - Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for Infant Sleep Products
Consumer productReported July 3, 2026 · The recalled baby loungers violate the mandatory safety standard for infant sleep products. The sides are too low to contain an infant and the enclosed... - 25# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/NS recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 5# Sunflower Seeds C/S recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 8/9.5oz Tub Nut - Sunflower Seed recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz No Salt Sunflower Seeds recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 6/11oz Sunflower Seeds Salted recall (George J Howe Company, Inc.)
FoodClass IReported July 1, 2026 · The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew. - 2.0 oz Dirty Sour Cream and Onion Potato Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.0 oz Dirty Maui Onion Chip recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 2.5oz recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - 1.5oz Zapp's Bayou Blackened Ranch Kettle Chips recall (Utz Quality Foods, LLC)
FoodClass IReported July 1, 2026 · Potential presence of Salmonella. - Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green... recall (Produce Innovations)
FoodClass IIIReported July 1, 2026 · Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich - Dried Herring Fish 7 oz. recall (Prime Food Processing LLC.)
FoodClass IReported July 1, 2026 · Improperly eviscerated which may result in Clostridium botulinum contamination - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. KIT... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 1, 2026 · Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. - INZONE DETACHMENT SYSTEM recall (Stryker Neurovascular)
Medical deviceClass IIReported July 1, 2026 · Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and... - Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe... recall (Acumed LLC)
Medical deviceClass IIReported July 1, 2026 · Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Da Vinci ASSY recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported July 1, 2026 · Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would... - Spring & Mulberry Blood Orange Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Coffee Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Sea Salt Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - 1) Spring & Mulberry Pure Dark Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Pecan Date Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination. - Spring & Mulberry Mulberry Fennel Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination. - Spring & Mulberry Mango Chili Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Lavender Rose Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Earl Grey Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Mixed Berry Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Spring & Mulberry Mint Leaf Date-Sweetened Chocolate recall (Spring & Mulberry Inc.)
FoodClass IReported July 1, 2026 · Potential Salmonella contamination - Motor City Pizza Co. 5 Cheese Bread Single retail pack recall (Champion Foods, LLC)
FoodClass IIReported July 1, 2026 · potential salmonella contamination - Perampanel CIII Tablets recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIReported July 1, 2026 · Labeling: Label Mix-up: 10mg Perampanel CIII tablet was found in a Perampanel CIII bottle labeled Perampanel 6 mg tablets. - Povi-One recall (Elevate Oral Care)
DrugClass IIReported July 1, 2026 · sub potency - Lacosamide Tablets recall (Annora Pharma Private Limited)
DrugClass IIReported July 1, 2026 · Presence of a Foreign Tablets: Complaint received, possible mix-up of Selexipag 1000 mcg tablet in a bottle of Lacosamide Tablets USP, 100mg. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - hydrOXYzine Hydrochloride Oral Solution recall (ANI Pharmaceuticals, Inc.)
DrugClass IIIReported July 1, 2026 · Presence of foreign substance - DULOXETINE D/R recall (Direct Rx)
DrugClass IIReported July 1, 2026 · CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Sensipar recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Corlanor recall (Amgen, Inc.)
DrugClass IIReported July 1, 2026 · Presence of Foreign Substance. - Fenofibrate Capsules recall (Ajanta Pharma USA Inc)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Carton Label: MAJOR recall (The Harvard Drug Group LLC)
DrugClass IIReported July 1, 2026 · Subpotent Drug - Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 1, 2026 · There is the potential for leakage along the drug pathway from the pump through the end of the catheter. - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). - Surgify Halo recall (SURGIFY MEDICAL OY)
Medical deviceClass IIReported July 1, 2026 · Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).