The Recall Desk

State

Washington product recalls

73,824 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,536
Critical
865
Severe
2,405
Most recent
2026-11-04

Of the 8,536 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 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46426–46450 of 82360

  • ModerateFDA (Devices)·Z-2966-2017·2017-08-16

    Valorem Surgical Recalls Pallas M/MAXIMIS Nut Drivers for Quality Issues

    Valorem Surgical LLC is recalling 262 units of Pallas M/MAXIMIS Nut Drivers because they are not consistent with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS Nut Driver 4.0 Hexa and Alignment Driver. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2919-2017·2017-08-16

    Valorem Surgical Recalls Pallas M Pedicle Screws for Quality System Issues

    Valorem Surgical LLC is recalling 2,225 Pallas M/MAXIMIS MIS Pedicle Screws because they are not consistent with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS MIS Screw 7.5 x 40mm. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2841-2017·2017-08-16

    FDA Recalls Piston Syringes Due to Insufficient Sterility Documentation

    International Medsurg Connection is recalling 54.2 million piston syringes and hypodermic needles because the company lacks documentation to support the products' sterility claims.

    Product
    Piston Syringe and Hypodermic Needle, 5 CC L/L 21 G X 1.5, 100 per box, 15 boxes/case, 1,500/case The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2958-2017·2017-08-16

    Valorem Surgical Recalls Pallas M/MAXIMIS 350 Straight Rods for Quality Issues

    Valorem Surgical LLC is recalling 2,225 Pallas M/MAXIMIS 350 Straight Rods because the devices are not consistent with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS 350 Straight Rod. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3017-2017·2017-08-16

    Elekta Recalls iGUIDE Software 2.2 Due to Incorrect PEC Values

    Elekta, Inc. is recalling iGUIDE Software 2.2 because it contains incorrect PEC values. The software is used for patient positioning in radiotherapy environments.

    Product
    iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-2982-2017·2017-08-16

    Valorem Surgical Recalls Pallas M/MAXIMIS MIS Tapper 5.5mm Spinal Fixation Devices

    Valorem Surgical LLC is recalling 262 units of the Pallas M/MAXIMIS MIS Tapper 5.5mm because the devices are not consistent with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS MIS Tapper 5.5mm. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2995-2017·2017-08-16

    Valorem Surgical Recalls Pallas M Rod Bender for Quality System Issues

    Valorem Surgical LLC is recalling 262 Pallas M/MAXIMIS Rod Benders because they are not consistent with Quality System Requirements. The devices are used for spinal fixation.

    Product
    PALLAS M/MAXIMIS Rod Bender. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2969-2017·2017-08-16

    Valorem Surgical Recalls Pallas M Rod Bender for Quality Issues

    Valorem Surgical LLC is recalling 262 Pallas M/MAXIMIS Rod Benders because they are not consistent with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS Rod Bender. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2816-2017·2017-08-16

    FDA Recalls Hypodermic Needles Due to Insufficient Sterility Documentation

    International Medsurg Connection is recalling 54.2 million hypodermic needles because the company lacks sufficient documentation to support the products' sterility claims.

    Product
    Hypodermic Needle, 23 G X 1.0 in REG BEVEL, 100 per box, 50 boxes/case, 5,000/case The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2945-2017·2017-08-16

    Valorem Surgical Recalls Pallas M/MAXIMIS 70mm Curved Rods

    Valorem Surgical LLC is recalling 2,225 Pallas M/MAXIMIS 70mm Curved Rods due to non-compliance with Quality System Requirements.

    Product
    PALLAS M/MAXIMIS 70mm Curved Rod. Part of MAXIMIS Pedicle Screw Spinal Fixation System. Valorem Surgical, Chicago, IL. Product labeled as Pallas M Spinal Fixation System through 2015. Intended for posterior pedicle screw fixation of the non-cervical spine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17207·2017-08-15

    BRIO Recalls Soft Hammer Baby Rattles Due to Choking Hazard

    BRIO is recalling soft hammer baby rattles because wooden rings can crack, posing a choking hazard to children. No injuries have been reported.

    Product
    BRIO soft hammer rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17206·2017-08-15

    Laura Ashley Girl's Dresses Recalled Due to Choking Hazard

    Pastourelle is recalling Laura Ashley girl's dresses because flower petals can detach, posing a choking hazard to children.

    Product
    Girl's dresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V505000·2017-08-14

    Keystone Recalls 2018 Crossroads Trailers Due to Propane Line Fire Risk

    Keystone RV is recalling 2018 Crossroads Redwood and Cameo trailers because the propane manifold may contact the floor, potentially damaging the line and causing a leak that increases fire risk.

    Product
    CROSSROADS — CROSSROADS CAMEO, REDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V502000·2017-08-14

    BMW Recalls 2014-2017 R NINE T Motorcycles for Swingarm Bolt Issue

    BMW is recalling 2014-2017 R NINE T motorcycles because swingarm pivot pin bolts may loosen, increasing crash risk. Dealers will repair the issue free of charge.

    Product
    BMW — BMW R NINE T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V506000·2017-08-14

    Mercedes-Benz Recalls AMG GLE43 Vehicles Due to Engine Shutdown Risk

    Mercedes-Benz is recalling 2016-2017 AMG GLE43 vehicles because software conflicts may cause the engine to shut down while driving, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V406000·2017-08-14

    2018 International LT and HX Trucks Recalled for Fuel Pump Defect

    Navistar is recalling 2018 International LT and HX trucks because a fuel pump gear may slip, causing engine stalls that increase crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, HX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V504000·2017-08-14

    KME Predator Aerial Vehicles Recalled for Ladder Speed Software Error

    KME is recalling 2012-2017 Predator Aerial vehicles because a software error may cause the ladder to accelerate unexpectedly, increasing injury risk.

    Product
    KME — KME PREDATOR SS AERIAL, PREDATOR AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V500000·2017-08-10

    Forest River Berkshire Recall: Battery Cable Fire Risk

    Forest River is recalling 2016-2017 Berkshire vehicles because an improperly installed battery cable bracket may cause chafing and short circuits, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V499000·2017-08-10

    AEV Recalls Modified RAM 2500 and 3500 Trucks Due to Wheel Fracture Risk

    Streetcar ORV LLC is recalling 2013-2017 RAM 2500 and 3500 trucks modified with specific cast aluminum wheels that may fracture, causing rapid air loss and potential loss of vehicle control.

    Product
    RAM — RAM 2500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V498000·2017-08-10

    Temsa Recalls 2014-2018 TS45 Buses Due to Steering Hose Leak Risk

    Temsa is recalling 2014-2018 TS45 coach buses because the tag axle steering hydraulic hose may leak or burst, potentially causing loss of control or fire.

    Product
    TEMSA — TEMSA TS45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17204·2017-08-10

    Kawasaki Recalls All-Terrain Vehicles Due to Fuel Leak Fire Hazard

    Kawasaki is recalling approximately 15,000 KFX50 and KFX90 all-terrain vehicles because a leaking fuel tap poses a fire hazard. No injuries have been reported.

    Product
    All-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2961-2017·2017-08-09

    Clif Builders Chocolate Mint Bars Recalled for Undeclared Peanuts and Tree Nuts

    Clif Bar & Company is recalling Clif Builders Chocolate Mint bars due to undeclared peanuts and/or tree nuts. The recall covers multiple pack sizes distributed nationwide and internationally.

    Product
    Clif Builders Chocolate Mint 12-count, 6-pack, 7-pack, Snack Size 200-count
    Category
    Food
    Distribution
    Distributed nationwide