The Recall Desk

State

Washington product recalls

73,738 recalls have nationwide distribution and so reach Washington. 8,535 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,535
Critical
865
Severe
2,404
Most recent
2026-10-28

Of the 8,535 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,404 (28%) are Severe.

These figures cover only the 8,535 recalls whose distribution notice names Washington specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33451–33475 of 82273

  • ModerateFDA (Drugs)·D-0799-2020·2020-01-29

    FDA Recalls NETSPOT Kits Due to Defective Aluminum Cap Crimp

    Advanced Accelerator Applications USA, Inc. is recalling NETSPOT kits because the dilution buffer vial has a loose aluminum cap crimp.

    Product
    NETSPOT — NETSPOT (68GA-DOTATATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0818-2020·2020-01-29

    Greiner Bio-One Recalls Damaged Vacuette Blood Collection Tubes

    Greiner Bio-One is recalling 1,002,000 Vacuette tubes that may have cap sealing damage, potentially causing vacuum loss and improper blood volume collection.

    Product
    VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles are use together as a system for the collection of venous blood. VACUETTE tubes are used to collect, transport, and process blood for testing serum, plasma, or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V047000·2020-01-28

    Mercedes-Benz Recalls 2019 AMG GT63 Models Due to Wiring Harness Issue

    Mercedes-Benz is recalling 2019 AMG GT63 and GT63S vehicles because a transmission wiring harness may chafe against the drive shaft, potentially causing an engine stall.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT 63, AMG GT63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V048000·2020-01-27

    Mercedes-Benz Recalls AMG Models Due to Turbocharger Oil Leak Fire Risk

    Mercedes-Benz is recalling certain 2018-2019 AMG vehicles because a turbocharger oil feed line may leak, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT63, AMG S63, AMG E63S, AMG GT 63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2020·2020-01-24

    Golden Pearl Trading Recalls Imported Salted Egg Fish Skin Products

    Golden Pearl Trading Corporation is recalling approximately 12,054 pounds of ready-to-eat imported salted egg fish skin products that were not presented for import re-inspection.

    Product
    Golden Pearl Trading Corporation Recalls Ready to Eat Imported Siluriformes Products Produced Without Benefit of Import Inspection
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·20V043000·2020-01-24

    Chrysler Recalls 2019-2020 Ram 2500 and 3500 for Fire Risk

    Chrysler is recalling 2019-2020 Ram 2500 and 3500 pickups because transmission fluid leaks may contact ignition sources, increasing the risk of a fire.

    Product
    RAM — RAM 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V037000·2020-01-23

    Keystone Recalls 2020 Crossroads Trailers Due to Wiring Fire Risk

    Keystone RV is recalling 2020 Crossroads trailers because improper WiFi wiring circuit protection may increase the risk of fire during a short circuit.

    Product
    CROSSROADS — CROSSROADS VOLANTE, HAMPTON, CAMEO, SUNSET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V036000·2020-01-23

    Ram ProMaster Recall: Transmission Shifter Cable May Disconnect

    Chrysler is recalling 2014-2019 Ram ProMaster vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V038000·2020-01-23

    GM Recalls 2014-2015 Cadillac CTS-V Sport for Rear Axle Defect

    General Motors is recalling 2014-2015 Cadillac CTS-V Sport vehicles because rear-axle differential roll pins may fracture, potentially causing the driver to lose control.

    Product
    CADILLAC — CADILLAC CTS-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V040000·2020-01-23

    Rosenbauer Commander Recall: Front Shocks May Separate and Damage Steering

    Rosenbauer America is recalling 2014-2019 Commander vehicles because front shocks may separate, potentially damaging the steering gear and causing a loss of power steering assist.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0864-2020·2020-01-22

    Hikma Recalls Ketorolac Tromethamine Injection Due to Particulate Matter

    Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0514-2020·2020-01-22

    FDA Recalls Butler's Dark Chocolate with Irish Whisky for Undeclared Milk

    Gourmet International Ltd. is recalling Butler's Dark Chocolate with Irish Whisky bars due to undeclared milk. The recall affects 2,000 units distributed across 15 states.

    Product
    Butler's Dark Chocolate with Irish Whisky, 3.52oz bar, UPC 8 44984 17619 7, 10 units per case
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-0695-2020·2020-01-22

    Assurance Infusion Recalls BUP 21MG/CLON 252MCG/MORP 20MG/ML Injection Syringes

    Assurance Infusion is recalling BUP 21MG/CLON 252MCG/MORP 20MG/ML Injection syringes due to a lack of sterility assurance. The recall covers products distributed nationwide.

    Product
    BUP 21MG/CLON 252MCG/MORP 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0744-2020·2020-01-22

    Assurance Infusion Recalls Hydromorphone Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Hydromorphone 3mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.

    Product
    HYDROMORPHONE 3MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0757-2020·2020-01-22

    Assurance Infusion Recalls Morphine Syringes Due to Sterility Concerns

    Assurance Infusion is recalling specific lots of Morphine 30mg/mL injection syringes due to a lack of sterility assurance. The affected products were distributed nationwide.

    Product
    MORPHINE 30MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800
    Category
    Drug
    Distribution
    Distributed nationwide