The Recall Desk

State

Washington product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32301–32325 of 82272

  • ModerateFDA (Devices)·Z-1645-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 145 MM, Silicone, Sterile, Item 431192.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1662-2020·2020-04-15

    Biomet Recalls Knee Spacer Molds Due to Insufficient Cleaning Process

    Biomet, Inc. is recalling 230,001 units of StageOne Knee Femoral Cement Spacer Molds due to a potentially insufficient cleaning process or inadequate process monitoring.

    Product
    BIOMET StageOne Knee Femoral Cement Spacer Mold, 60 MM, Silicone, Sterile, Item 432160.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1648-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet, Inc. is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 200 MM, Silicone, Sterile, Item 431195.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1651-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet, Inc. is recalling specific lots of StageOne Select Hip Stem Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 15 X 200 MM, Silicone, Sterile, Item 431198.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1690-2020·2020-04-15

    Microbiologics Recalls KWIK-STIK Trichosporon Dermatis Culture Pack

    Microbiologics Inc is recalling KWIK-STIK 2 Pack Trichosporon dermatis cultures because they may contain Candida utilis instead of the labeled organism.

    Product
    KWIK-STIK 2 Pack Trichosporon dermatis derived from ATCC 204094 (Catalog# 0778P, lot 778-65-3)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1656-2020·2020-04-15

    Biomet Hip Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes and inadequate process monitoring.

    Product
    BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 17 X 165 MM, 64 MM, Silicone, Sterile, Item 431217.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1639-2020·2020-04-15

    Biomet Recalls StageOne Hip Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 units of StageOne Hip Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 52 MM, Silicone, Sterile, Item 431182.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1650-2020·2020-04-15

    Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 13 X 200 MM, Silicone, Sterile, Item 431197.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1657-2020·2020-04-15

    Biomet Shoulder Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling 230,001 units of StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.

    Product
    BIOMET StageOne, Shoulder Cement Spacer Mold 6 MM, 42 X 18 X 46 MM, Silicone, Sterile, Item 431406.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1665-2020·2020-04-15

    Biomet Knee Spacer Mold Recalled for Potential Cleaning Deficiencies

    Biomet is recalling StageOne Knee Femoral Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Knee Femoral Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 432175.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1672-2020·2020-04-15

    Qualigen FastPack SHBG Immunoassay Kit Recalled for Inaccurate Results

    Qualigen Inc is recalling FastPack System Complete Immunoassay Kits for SHBG because they may produce higher than expected results, leading to inaccurate quantitative determinations.

    Product
    The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative Measurement of SHBG is a chemiluminescent immunoassay intended for the quantitative determination of Sex Hormone Binding Globulin in human serum and plasma on the FastPack System. The FastPack IP…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1667-2020·2020-04-15

    Biomet Recalls Knee Tibial Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 units of StageOne Knee Tibial Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.

    Product
    BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1686-2020·2020-04-15

    Baxter Recalls GEM Microvascular Couplers Due to Labeling Mismatch

    Baxter Healthcare is recalling 209 GEM Microvascular Anastomotic Coupler Devices because the size labeling on the outer tray may not match the inner tray.

    Product
    GEM Microvascular Anastomotic Coupler Devices - Product Usage: s intended to be used in the anastomosis of veins and arteries normally encountered in microsurgical procedures only in the peripheral vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1661-2020·2020-04-15

    Biomet Shoulder Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne, Shoulder Cement Spacer Mold 14 MM, 58 X 24 X 64 MM, Silicone, Sterile, Item 431414.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1687-2020·2020-04-15

    Baxter Recalls GEM Microvascular Couplers Due to Labeling Mismatch

    Baxter Healthcare is recalling GEM Microvascular Anastomotic Coupler Devices because the size labeling on the outer tray may not match the inner tray.

    Product
    GEM Microvascular Anastomotic Coupler Devices s intended to be used in the anastomosis of veins and arteries normally encountered in microsurgical procedures only in the peripheral vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1670-2020·2020-04-15

    Biomet Recalls Custom StageOne Hip Femoral Reinforcement Due to Cleaning Concerns

    Biomet, Inc. is recalling specific lots of Custom StageOne Hip Femoral Reinforcement due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET Custom StageOne Hip Femoral Reinforcement, 9 X 125 MM, Stainless Steel, PMI Instrument, Sterile, Item CP161972.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1666-2020·2020-04-15

    Biomet Recalls Knee Tibial Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling 230,001 units of StageOne Knee Tibial Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.
    Category
    Medical Device
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1644-2020·2020-04-15

    Biomet Hip Stem Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes and inadequate monitoring.

    Product
    BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 135 MM, Silicone, Sterile, Item 431191.
    Category
    Medical Device
    Distribution
    49 states
  • HighNHTSA·20V214000·2020-04-14

    Commercial Truck Rear Reflective Tape Obstruction Creates Visibility Risk

    Daimler Trucks is recalling certain commercial trucks where the mudflap hanger bracket partially covers rear reflective tape, reducing visibility. Owners should contact DTNA or NHTSA for free inspection and repositioning.

    Product
    FREIGHTLINER — FREIGHTLINER, STERLING, WESTERN STAR FLD, COLUMBIA, CLASSIC XL, 122SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E022000·2020-04-13

    Takata Driver Air Bag Inflator Recall for Honda and Nissan Vehicles

    Honda and Nissan are recalling vehicles with Takata driver air bag inflators that may explode during deployment, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2020·2020-04-10

    Conagra Recalls Frozen Chicken Bowls Due to Possible Rock Contamination

    Conagra Brands is recalling approximately 130,763 pounds of frozen Healthy Choice Chicken Feta & Farro bowls because they may contain small rocks.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-to-Eat Chicken Bowl Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20E021000·2020-04-10

    Winkelmann CNG Cylinder Label Recall for Inspection Compliance

    Winkelmann Flowform Technology LP is recalling 327-liter compressed natural gas cylinders because label font size and missing designations may prevent inspection, increasing fire risk.

    Product
    EQUIPMENT:OTHER:LABELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V211000·2020-04-10

    Freightliner and Western Star trucks recalled for incorrect weight rating labels

    Daimler Trucks North America is recalling 2020-2021 Freightliner and Western Star commercial trucks with incorrect weight-rating labels. Incorrectly labeled trucks could be overloaded, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CORONADO, 114SD, 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V213000·2020-04-09

    Hyundai Recalls 2020 Nexo and Sonata for Parking Software Defect

    Hyundai is recalling 2020 Nexo and Sonata vehicles because a software defect in the Remote Smart Parking Assist system may allow unintended vehicle movement, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI NEXO, SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V209000·2020-04-09

    Forest River Recalls 2021 Starcraft Bus All Star Over Wiring Chafing

    Forest River is recalling 2021 Starcraft Bus All Star transit buses because a wire harness may chafe against the frame, potentially causing engine stalls or loss of braking stability.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALL STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide