Recalls in Washington (page 10)
4037 recalls.
- Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE... recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or... - Medline Convenience Kits: 1) BLOOD DRAW KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ORTHO ASPIRATION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) EYE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) C-SECTION PREP recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) LABOR CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) PRE-OP KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT LAB DRAW-SH recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ARTERIAL LINE INSERTION KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IV START KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) ULTRASOUND BREAST PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) COLORECTAL ME recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) IVS BLOOD CULTURE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DYKM1414 recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) CDS840396X recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT recall (Medline Industries, LP)
Medical deviceClass IIReported September 9, 2026 · The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in... - 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 - MONDRAKER USA Recalls Mountain Bicycles Equipped with ONOFF S9 Carbon MTB Handlebars Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported September 3, 2026 · The affected handlebars may crack or fracture during use, which can lead to loss of control, posing a risk of serious injury or death from fall hazard. - Clorox Puerto Rico Recalls 6 Million Scented Mistolin and Lestoil Multi-Purpose Cleaners Due to Risk of Exposure to Bacteria
Consumer productReported September 3, 2026 · The recalled products may contain bacteria, including Pseudomonas aeruginosa, which is an environmental organism found widely in soil and water. People with... - Truststone Group Recalls XO Poppy Power Trip Magnetic Wireless Power Banks Due to Fire and Burn Hazards; Sold Exclusively at TJX and Marshalls Stores
Consumer productReported September 3, 2026 · The lithium-ion battery in the recalled power banks can overheat and ignite, posing fire and burn hazards to consumers. - Skip Hop Recalls Baby Sesame Street Elmo Silicone Teethers Due to Risk of Serious Injury or Death from Choking Hazard
Consumer productReported September 3, 2026 · The black eyes can detach from the recalled teether if frozen, posing a risk of serious injury or death from a choking hazard. - GIHNJSI Squeezy Dumplings Toys Recalled Due to Serious Ingestion, Choking and Obstruction Hazards; Sold on Amazon by Chenyuanhui
Consumer productReported September 3, 2026 · The squeezy toys contain water beads. If ingested, water beads expand and can pose deadly ingestion, choking, and intestinal obstruction hazards inside a... - OKK Trading Recalls Rainbow Mystery Squishy Bun Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
Consumer productReported September 3, 2026 · The squishy bun toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly... - Gizoon Direct Recalls Six-Drawer Double Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Consumer productReported September 3, 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... - Branch Recalls Ergonomic Chairs Due to Fall Hazard
Consumer productReported September 3, 2026 · The backrests of the chairs can detach, posing a fall hazard to consumers. - Daikin Comfort Technologies Manufacturing Recalls Amana Through-The-Wall Air Conditioners and Heat Pumps Due to Risk of Serious Injury from Fire
Consumer productReported September 3, 2026 · The snubber circuit can emit flames if it shorts, posing a risk of serious injury due to fire hazard. - Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Loyoda Direct and Loyoda
Consumer productReported September 3, 2026 · The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed... - SHEIN Distribution Corporation Recalls Spiral Toys Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Ball Ban
Consumer productReported September 3, 2026 · The toys violate the small ball ban because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard. - Audio Partnership Recalls Cambridge Audio Yoyo (M) Portable Bluetooth Speakers Due to Fire Hazard
Consumer productReported September 3, 2026 · The lithium-ion batteries in the Cambridge Audio Yoyo (M) Portable Bluetooth Speaker can overheat, posing a fire hazard. - Nanjing Wu Hai Smart Home Appliance Store Recalls Alanca 6-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 3, 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... - Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts recall (Byron White Formulas, Inc.)
FoodClass IIReported September 2, 2026 · Label does not declare walnuts in English - bettergoods brand Pistachio Nut Butter recall (Botticelli Foods, LLC)
FoodClass IReported September 2, 2026 · Product may be contaminated with Salmonella. - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Black Cherry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Tangerine recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Grape recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bar Watermelon recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - Outshine Fruit Bars Strawberry recall (Dreyer's Grand Ice Cream Inc.)
FoodClass IIReported September 2, 2026 · Foreign object: products may contain glass pieces - BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING recall (KHONG GUAN (HQ))
FoodClass IReported September 2, 2026 · Undeclared peanuts. - Glutinous Rice Balls with Black Sesame Filling recall (KHONG GUAN (HQ))
FoodClass IReported September 2, 2026 · Undeclared peanuts. - Merge PACS and Merge OrthoPACS recall (Merge Healthcare, Inc.)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause measurements to be displayed inaccurately. - Horizon Organic ORG ASEP CHOC MILK 1% 8OZ 12 CT recall (Horizon Organic Dairy, LLC)
FoodClass IIReported September 2, 2026 · Product has the potential to be spoiled. - Lactated Ringer's Injection USP recall (B BRAUN MEDICAL INC)
DrugClass IReported September 2, 2026 · Presence of Particulate matter. - Ramipril Capsules USP recall (Hikma Pharmaceuticals USA INC.)
DrugClass IIReported September 2, 2026 · Failed Impurities/Degradation Specifications: OOS result obtained for a process impurity, dicyclohexylurea (DCU). - Tyenne recall (Fresenius Kabi USA, LLC)
DrugClass IReported September 2, 2026 · Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles. - Paxil CR recall (Apotex Corp.)
DrugClass IIReported September 2, 2026 · Failed Dissolution Specifications; product failed to meet 24-month stability testing acceptance criteria - Acthar Gel recall (Mallinckrodt Hospital Products Inc.)
DrugClass IIReported September 2, 2026 · Presence of particulate matter: glass and stopper piece - Zicam recall (Church & Dwight Co., Inc.)
DrugClass IIReported September 2, 2026 · CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing - Clobetasol Propionate Cream USP recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported September 2, 2026 · Failed content uniformity specifications. - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - Levothyroxine Sodium Tablets recall (ACCORD HEALTHCARE, INC.)
DrugClass IIReported September 2, 2026 · Subpotent Drug - POWERSEAL 5 MM recall (Olympus Corporation of the Americas)
Medical deviceClass IIReported September 2, 2026 · Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device. - ORT300 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - ORT200 recall (IMRIS Imaging Inc)
Medical deviceClass IIReported September 2, 2026 · The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and... - healthmark ProChek-W Protein Test for Robotic Arms recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - healthmark ProChek-II recall (Healthmark Industries Co., Inc.)
Medical deviceClass IIReported September 2, 2026 · Test manufactured with an expired ingredient which may present as either a false negative or positive. - FUJIFILM Synapse PACS software v7.4.310 recall (FUJIFILM Healthcare Americas Corporation)
Medical deviceClass IIReported September 2, 2026 · Software issue may cause the ruler measurement to be inaccurate. - Medline convenience kits labeled as: 1) LAMI FUSION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) LAVH recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) C-SECTION recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) GYN ROBOTIC CDS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR GYN PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: LTP CDS-LF recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) MAJOR PROCEDURE recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) OPEN HEART PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - Medline convenience kits labeled as: 1) FEMORAL PACK recall (Medline Industries, LP)
Medical deviceClass IIReported September 2, 2026 · Kits contain a potentially contaminated component which were recalled by the manufacturer - CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B... recall (ConMed Corporation)
Medical deviceClass IIReported September 2, 2026 · Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability. - Fresenius Medical Care recall (Fresenius Medical Care Renal Therapies Group, LLC)
Medical deviceClass IIReported September 2, 2026 · Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ ... - Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Structur 2 SC Temporary Resin Cartridge Refill 75Gm recall (Henry Schein Inc.)
Medical deviceClass IIReported September 2, 2026 · Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. - Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital... recall (Canon Medical System, USA, INC.)
Medical deviceClass IIReported September 2, 2026 · Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose. - Midmark Digital ECG HD+12 recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Midmark IQecg Digital ECG recall (Midmark Corporation)
Medical deviceClass IIReported September 2, 2026 · A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03 recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. - Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY... recall (AVID Medical, Inc.)
Medical deviceClass IIReported September 2, 2026 · Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.