Recalls in California (page 9)
4209 recalls.
- Esjay US Recalls Toddler Busy Board Montessori Toys Due to Risk of Serious Injury or Death from Choking; Violates Small Parts Ban
Consumer productReported September 17, 2026 · The recalled toy violates the small parts ban because the product is for children under three years of age and the red knobs can detach, posing a deadly... - Colerinsec Recalls Jerify Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 17, 2026 · The magnetic humanoid toy Sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to... - Char-Broil Recalls Bistro Pro Electric Grills Due to Risk of Electric Shock
Consumer productReported September 17, 2026 · The grounding wire for the grill's heating element can disconnect and lose fault protection, posing an electric shock hazard. - Alfalfa recall (International Sprout Holdings, Inc)
FoodClass IReported September 16, 2026 · Potential E. coli and Salmonella contamination - AMS Convenience Kit: DSAEK Pack - RX recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IIReported September 16, 2026 · The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that... - HeartSine SAM 350P 350P US Device recall (HeartSine Technologies Ltd)
Medical deviceClass IIReported September 16, 2026 · Due to a damaged (over stretched) membrane tail that causes an intermittent fault. - Products that contain the Pericare Wipes: recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF:... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray ... recall (C.R. Bard Inc)
Medical deviceClass IIReported September 16, 2026 · Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays. - Prolon Everyday Apulian Almond & Cocoa Spread recall (L-Nutra Inc)
FoodClass IIReported September 16, 2026 · Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio. - 0.9% Sodium Chloride Injection recall (B BRAUN MEDICAL INC)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene - Epinephrine Injection recall (American Regent, Inc.)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and... - fentaNYL Citrate recall (OurPharma LLC)
DrugClass IIReported September 16, 2026 · Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product... - Dextrose Injection recall (Baxter Healthcare Corporation)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. - Fluphenazine Hydrochloride Tablets recall (Ajanta Pharma USA Inc)
DrugClass IIIReported September 16, 2026 · Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result... - Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution recall (ImprimisRx NJ LLC)
DrugClass IIIReported September 16, 2026 · Subpotent Drug - Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Bicarbonate Powder REF: DB+201-2.1 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 recall (Nipro Renal Soultions USA, Corporation)
Medical deviceClass IIReported September 16, 2026 · Hemodialysis concentrates contain high endotoxin levels - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Getinge PVC Thoracic Catheter recall (Atrium Medical Corporation)
Medical deviceClass IIReported September 16, 2026 · An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters. - Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser... recall (Lutronic Corporation)
Medical deviceClass IIReported September 16, 2026 · Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in... - Halyard IV Start Kit Non-Sterile REF: KRIV26-02 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 16, 2026 · Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper... - Bravo CF capsule delivery device recall (Given Imaging Ltd.)
Medical deviceClass IReported September 16, 2026 · Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus... - ZMC Group Expands Recall of Light-Up Children’s Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 10, 2026 · The recalled light-up toys violate the mandatory safety standard for children’s toys because the toys contain button cell batteries that can be easily accessed... - FJTJBSI Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Consumer productReported September 10, 2026 · 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... - Triumph Motorcycles Recalls Closed Course Competition Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard
Consumer productReported September 10, 2026 · The engine rocker arm on the recalled motorcycles can seize or stick and the exhaust valves can remain open or break, posing a risk of serious injury or death... - Cade California Electronic Recalls Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 10, 2026 · The recalled finger lights violate the mandatory safety standard for toys because the toys contain button cell batteries that can be easily accessed by... - Dual Fuel Ranges Recalled Due to Risk of Serious Injury or Death from Fire or Explosion Hazards; Manufactured by AGA Rangemaster
Consumer productReported September 10, 2026 · Dual Fuel Ranges with a missing cap from the gas test port can cause a gas leak, posing a risk of serious injury or death from fire or explosion hazards. - Prepared Hero Recalls Fire Spray Canisters Due to Risk of Serious Injury or Death from Fire and Burn Hazards
Consumer productReported September 10, 2026 · The recalled fire spray canister can deteriorate overtime, causing it to rupture and fail to operate during a fire, posing the risk of serious injury or death... - Guang Zhou Recalls Wantefully Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, Shock and Burn Hazards; Violate Federal Regulations
Consumer productReported September 10, 2026 · The recalled hair dryer brushes are in violation of federal regulations for hair dryers as they lack an integrated immersion protection device, which presents... - SQT Recalls Lontcs Busy Boards Due to Risk of Serious Injury from Lead Poisoning; Violate Federal Lead Paint Ban
Consumer productReported September 10, 2026 · The toys’ zipper contains levels of lead that exceed the standard set in the federal lead paint ban. Lead is toxic if ingested by young children and can cause... - Sweet Cubby Recalls Children's Loungewear Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear
Consumer productReported September 10, 2026 · The recalled children’s loungewear sets violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death. - Junkins Recalls DHASUWT Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, and Shock Hazards; Violate Federal Regulations; Smoking and Fire Hazards
Consumer productReported September 10, 2026 · The recalled hair dryer brushes lack an integrated immersion protection device, which presents a substantial product hazard to consumers, posing the risk of... - Victgoal Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets
Consumer productReported September 10, 2026 · The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system, positional... - Ricky Joy Recalls More Than 2.3 Million Sour Crush Candy Bottles Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported September 10, 2026 · The rolling ball on the recalled candy bottles can detach, posing a risk of serious injury or death from choking hazard. - OLA-OLA Pounded Yam recall (Fayus Inc.)
FoodClass IReported September 9, 2026 · Undeclared milk. - Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog... recall (B Braun Medical Inc)
Medical deviceClass IIReported September 9, 2026 · Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. - 5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - 5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - HEALON EndoCoat PRO recall (Johnson & Johnson Surgical Vision, Inc.)
Medical deviceClass IIReported September 9, 2026 · Surgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is encountered... - STA Staclot Protein S recall (Diagnostica Stago, Inc.)
Medical deviceClass IIReported September 9, 2026 · A positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified - Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - 1) NEURO recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - Halyard medical convenience kits labeled as: 1) ENT recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 9, 2026 · The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile... - THE HAMPTON GROCER brand recall (THE HAMPTON GROCER)
FoodClass IReported September 9, 2026 · Product may be contaminated with Salmonella. - Glutathione 200 mg/mL recall (OPTIMAL BALANCE PHARMACY)
DrugClass IReported September 9, 2026 · Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. - Prasugrel HCI recall (Golden State Medical Supply Inc.)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications. Notification from the manufacturer that lot is being recalled due to failed dissolution - Buprenorphine Sublingual Tablets recall (American Health Packaging)
DrugClass IIIReported September 9, 2026 · Labeling: Label Mix-up - Prasugrel Tablets recall (Mylan Pharmaceuticals Inc)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications; product failed to meet 18-month stability testing acceptance criteria - 2% Chlorhexidine Gluconate* Cloth recall (Sage Products, LLC)
DrugClass IIReported September 9, 2026 · Cross Contamination with Other Products - traZODone Hydrochloride Tablets recall (Teva Pharmaceuticals USA, Inc)
DrugClass IIReported September 9, 2026 · Presence of Foreign Tablets/Capsules - Trokendi XR recall (Supernus Pharmaceuticals, Inc.)
DrugClass IIIReported September 9, 2026 · Failed dissolution specifications. - Carton label: Mycophenolate Mofetil for injection recall (Mylan Pharmaceuticals Inc)
DrugClass IIReported September 9, 2026 · Failed Dissolution Specifications - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - THE ONE SPF 50 INVISIBLE SUNSCREEN GEL recall (Allies Group Inc.)
DrugClass IIReported September 9, 2026 · Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. - Doxylamine Succinate and Pyridoxine HCl Delayed-Release tablets 10 mg/10 mg recall (Bionpharma Inc.)
DrugClass IIIReported September 9, 2026 · Presence of Foreign Tablets/Capsules - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Phosphate in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Nexterone recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - CARDENE IV recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Pantoprazole Sodium in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Famotidine Injection in Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - MYXREDLIN recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported September 9, 2026 · The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a... - Citrasate recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - NaturaLyte recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product - GRANUFLO Dry Acid Concentrate: Product Numbers: 0FD2251-3B recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 9, 2026 · Complaints of blue-green discoloration in product