The Recall Desk

State

Washington product recalls

72,940 recalls have nationwide distribution and so reach Washington. 8,456 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,456
Critical
867
Severe
2,006
Most recent
2026-09-09

Of the 8,456 recalls naming Washington we have scored against our rubric, 867 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,006 (24%) are Severe.

These figures cover only the 8,456 recalls whose distribution notice names Washington specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3826–3850 of 81396

  • HighCPSC·26183·2026-01-15

    Energizer lanterns recalled because the lithium-ion battery can overheat

    About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.

    Product
    Energizer® Large Power Indicator Lanterns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V012000·2026-01-15

    Ford engine block heater may crack and short circuit when plugged in

    Ford is recalling certain 2016-2018 Focus, 2019 Explorer and 2024 Explorer vehicles because the engine block heater may crack and develop a coolant leak, causing a short circuit when plugged in.

    Product
    FORD — FORD FOCUS, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26192·2026-01-15

    Adirondack patio chairs recalled because they can crack and collapse

    About 6,100 Adams RealComfort and StyleWell Adirondack patio chairs are being recalled because the chairs can crack and collapse, posing injury and fall hazards.

    Product
    Adams RealComfort and StyleWell Adirondack Patio Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26191·2026-01-15

    Crib mattresses recalled because they may not fit certain cribs

    About 1,500 KEAWIS crib mattresses are being recalled because they may not adequately fit certain play yards or non-full-sized cribs, creating gaps that pose an entrapment hazard.

    Product
    KEAWIS Crib Mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0374-2026·2026-01-14

    Locatelli pecorino romano shippers recalled after testing positive for Listeria

    Ambriola is recalling 184 units of Locatelli Grated Pecorino Romano 48/8oz shippers after the product tested positive for Listeria monocytogenes.

    Product
    Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Devices)·Z-1001-2026·2026-01-14

    Organ recovery surgical packs recalled as not suitable for organ transplant

    AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1002-2026·2026-01-14

    Mini Plus surgical kits recalled as not suitable for organ transplant

    AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1000-2026·2026-01-14

    Organ recovery packs recalled as not suitable for organ transplant

    AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0289-2026·2026-01-14

    ClearLife allergy nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.

    Product
    CLEARLIFE EXTRA STRENGTH — CLEARLIFE EXTRA STRENGTH (ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0373-2026·2026-01-14

    Ambriola Piccante pecorino romano recalled after testing positive for Listeria

    Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.

    Product
    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Food)·H-0372-2026·2026-01-14

    Boar's Head pecorino romano in five pound bags recalled over Listeria

    Ambriola is recalling 405 five-pound bags of Boar's Head Pecorino Romano Grated after the product tested positive for Listeria monocytogenes.

    Product
    Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Drugs)·D-0288-2026·2026-01-14

    ReBoost nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.

    Product
    REBOOST — REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0353-2026·2026-01-14

    Spicy veggie breakfast burritos recalled over foreign material in 278 units

    Fresh & Ready Foods is recalling 278 units of Fresh to You Spicy Veggie Breakfast Burrito over foreign material.

    Product
    Spicy Veggie Breakfast Burrito, Fresh to You, Ready to Eat, Refrigerated. Net wt. 9.1oz. UPC 100000010310, LPK110310V06. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1027-2026·2026-01-14

    Patient monitors recalled over unvalidated intracranial and bladder pressure measurements

    Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0356-2026·2026-01-14

    Breakfast tacos recalled over foreign material in 200 units

    Fresh & Ready Foods is recalling 200 units of Evergreen Refreshments Eggs Potatoes Cheese Tacos over foreign material.

    Product
    Eggs Potatoes Cheese Tacos, Evergreen Refreshments brand, Ready to Eat, Refrigerated. Net wt. 6.3 oz. UPC 100040103898, EG03698v01. Fresh & Ready Foods, 701 Monster Rd, Renton, WA 98057.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1032-2026·2026-01-14

    Emergency call stations recalled over missing low battery alerts

    Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.

    Product
    Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
    Category
    Medical Device
    Distribution
    Distributed nationwide