The Recall Desk

State

Washington product recalls

20,324 recalls have nationwide distribution and so reach Washington. 0 additional recalls listed Washington specifically in their distribution scope.

About recalls in Washington

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Washington consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11851–11875 of 20324

  • HighFDA (Devices)·Z-2495-2023·2023-09-06

    Olympus Airway Mobilescope models may become lodged in connectors

    Olympus Airway Mobilescope endoscopes may become lodged in endotracheal tube connectors due to oversized diameter affecting airway management procedures nationwide.

    Product
    Olympus Airway Mobilescope, Models MAF-GM & MAF-TM.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1130-2023·2023-09-06

    Epinephrine IV Bags Recalled Due to Lack of Sanitization Validation

    Central Admixture Pharmacy Services is recalling epinephrine IV bags (Lot 36-260047) because sanitization processes lacked adequate validation data. The manufacturer cannot confirm the product meets sterility standards required for injectable medications.

    Product
    EPINEPHrine added to 0.9% sodium chloride, 4mg/250mL (16 mcg/mL), IV Bag, RX only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-8093-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2490-2023·2023-09-06

    Olympus Bronchovideoscope models recalled for lodging risk in airway connectors

    Olympus is recalling 1,715 Bronchovideoscope units across eight models due to a diameter defect that causes the device to lodge in the endotracheal tube connector.

    Product
    Olympus Bronchovideoscope, Models BF-1T150, BF-1T60, BF-MP60, BF-P150, BF-P60, BF-PE2, BF-TE2, BF-XT160.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1128-2023·2023-09-06

    Phenylephrine IV Injection Recalled for Lack of Sterility Assurance

    Central Admixture Pharmacy Services recalls phenylephrine IV bags nationwide because the manufacturer lacks validated sanitization data to ensure sterility. Healthcare providers should identify and quarantine affected inventory.

    Product
    PHENYLephrine added to 0.9% sodium chloride 50 mg/250mL (200mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043. NDC:72196-7039-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2471-2023·2023-09-06

    Laboratory diagnostic test may produce inaccurate results from reagent carryover

    Siemens is recalling the Atellica CH Total Bilirubin diagnostic test because reagent carryover on the analyzer could produce falsely elevated results affecting multiple related lab tests.

    Product
    Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma (lithium heparin) of adults and neonates Test Code: TBil_2 Siemens Material Number (SMN): 11097531
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2484-2023·2023-09-06

    Oculus Myopia Master optical device recalled for insufficient anti-reflective coating

    Oculus Optikgeraete GMBH is recalling 173 units of the Oculus Myopia Master optical measurement device due to insufficient anti-reflective coating that may cause incorrect axial length measurements.

    Product
    Oculus Myopia Master , Ref 68100, CE 0123
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1131-2023·2023-09-06

    EPINEPHrine IV bags recalled for sterility assurance failure

    Central Admixture Pharmacy Services recalled 554 bags of EPINEPHrine added to dextrose 5% IV bags nationwide due to insufficient validation of sanitization procedures, creating a lack of sterility assurance.

    Product
    EPINEPHrine added to dextrose 5%, 4mg/250ml (16 mcg/mL), IV Bag, Rx Only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Phoenix, AZ 85043, NDC: 72196-7018-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1118-2023·2023-09-06

    Neonatal TPN Starter Bags Recalled for Sterility Assurance Gaps

    Central Admixture Pharmacy Services is recalling 140 bags of Neonatal TPN Starter Bag due to lack of validation data for sanitization cycles. The injectable nutrition product was distributed nationwide.

    Product
    Neonatal TPN Starter Bag, Amino Acids (trophamine) 3%/Dextrose 10% with CALCIUM and HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0420-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1142-2023·2023-09-06

    Sabril (vigabatrin) oral solution recalled for cross-contamination

    Lundbeck LLC recalls Sabril (vigabatrin) oral solution nationwide due to potential cross-contamination. The recall affects 10,543 cartons.

    Product
    SABRIL — SABRIL (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1269-2023·2023-09-06

    Siemens Atellica CH Total Protein II Recalled for Reagent Carryover

    Siemens Healthcare Diagnostics is recalling Atellica CH Total Protein II due to reagent carryover affecting magnesium test accuracy. The recall covers all lots (13,071 units) distributed nationwide and internationally.

    Product
    Atellica CH Total Protein II- In vitro diagnostic use in the quantitative determination of total protein in human serum and plasma (lithium heparin) using the Atellica CH Analyzer. SMN: 11097604
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1139-2023·2023-09-06

    Clindamycin Phosphate Topical Solution Recalled for Defective Container

    Contract Pharmaceuticals is recalling Clindamycin Phosphate Topical Solution USP 1% due to defective containers that leak under the cap. The recall affects 11,350 bottles distributed nationwide.

    Product
    Clindamycin Phosphate Topical Solution USP, 1%, 60 mL bottle, Rx only, Manufactured by: Contract Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, Manufactured for: Glasshouse Pharmaceuticals Limited Canada, Mississauga, Ontario, Canada, NDC# 71428-003-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V333000·2023-09-05

    School bus structural joint defect poses crash protection risk

    Daimler Trucks North America is recalling Thomas Built school buses due to potentially insufficient rear interior joint strength. Dealers will add fasteners to reinforce the joints at no charge.

    Product
    THOMAS BUILT BUSES — 2023 THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V159000·2023-09-03

    Rivian R1S vehicles recalled for improperly secured side curtain air bags

    Rivian is recalling certain 2022-2023 R1S vehicles because fasteners securing the side curtain air bags may be improperly secured, potentially preventing proper deployment in a crash.

    Product
    RIVIAN — 2022 RIVIAN R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V170000·2023-09-03

    2022 Heartland Travel Trailers Recalled for Electrical Fire Risk

    Heartland is recalling certain 2022 Trail Runner, Prowler, and Lithium travel trailers with defective power inlet bolts that may loosen, creating an electrical fire hazard. Dealers will inspect and replace the inlet free of charge.

    Product
    HEARTLAND — 2022 HEARTLAND TRAIL RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V060000·2023-09-02

    RAM pickup and cab chassis trucks recalled for engine compartment fire risk

    Chrysler is recalling 2021–2023 RAM 2500, 3500, 4500, and 5500 Cummins diesel trucks due to an electrical short in the heater grid relay that can cause engine compartment fires. Owners should park outside and away from structures until repairs are completed.

    Product
    RAM — 2023 RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V059000·2023-09-02

    RAM 1500 and 2500 Rearview Display May Fail When in Reverse

    Certain 2021-2023 RAM 1500 and 2023 RAM 2500 vehicles have a software defect that may prevent the rearview image from displaying when in reverse, reducing driver visibility.

    Product
    RAM — 2022 RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V062000·2023-09-02

    Spartan Motorhome Chassis Software Error Causes Loss of Drive Power and Visibility

    Shyft Group is recalling 2022–2024 Spartan motorhome chassis due to a software error that may cause loss of drive power or safety functions like headlights and wipers. Owners should contact Shyft Group at 1-800-237-7806 for a free software update.

    Product
    SPARTAN — 2023 SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V058000·2023-09-02

    2022 Jeep Compass instrument panel display insufficient illumination during daytime

    The 2022 Jeep Compass instrument panel center cluster display may be insufficiently illuminated and may not be visible during daytime driving. This could prevent drivers from seeing safety-critical information like the fuel gauge and warning lights.

    Product
    JEEP — 2022 JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V061000·2023-09-02

    Motorhome Cooktops May Leak Gas and Create Fire Risk

    Forest River is recalling certain 2022-2023 Coachmen motorhomes with faulty cooktops. The burner tubes may fracture and leak gas, creating a fire hazard.

    Product
    COACHMEN — 2023 COACHMEN GALLERIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V064000·2023-09-02

    2023 Subaru Solterra: hub bolts may loosen and cause wheels to detach

    Certain 2023 Subaru Solterra vehicles have improperly tightened hub bolts that may loosen and cause wheel detachment. Owners should not drive until dealers complete repairs.

    Product
    SUBARU — 2023 SUBARU SOLTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23269·2023-08-31

    Frigidaire Gas Cooktops Recalled for Gas Leak and Fire Hazard

    Electrolux Group is recalling about 215 Frigidaire gas cooktops because plastic control knobs with black shafts can crack or break during use, creating a risk of gas leak and fire. Electrolux has received 63 reports of cracking or breaking, including one minor injury from a gas leak and one report of fire.

    Product
    Frigidaire Stainless-Steel 30-inch 4 Burner and 36-inch 5 Burner Gas Cooktops
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23788·2023-08-31

    Polaris MATRYX PRO RMK and MATRYX RMK KHAOS Snowmobiles Recalled for Puncture Hazard

    Polaris is recalling about 15,900 Model Year 2022–2023 MATRYX PRO RMK and MATRYX RMK KHAOS snowmobiles because handlebar hooks pose a puncture hazard and risk of serious injury during crashes. The firm has received four reports of puncture wounds.

    Product
    Polaris Snowmobiles, Model Year 2022-2023 MATRYX PRO RMK and MATRYX RMK KHAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23270·2023-08-31

    Apollo Phantom Electric Scooters Recalled for Fall and Injury Hazards

    Apollo Imports Inc. is recalling approximately 3,900 Apollo Phantom Electric Scooters because a stem bolt can come loose, causing the suspension and wheel assembly to separate and posing a fall and injury hazard. The company has received seven reports of bolt breaking, including three injuries.

    Product
    Apollo Phantom Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide