The Recall Desk

State

Washington product recalls

73,366 recalls have nationwide distribution and so reach Washington. 8,462 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total
8,462
Critical
868
Severe
2,396
Most recent
2026-10-07

Of the 8,462 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.

These figures cover only the 8,462 recalls whose distribution notice names Washington specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18126–18150 of 81828

  • HighFDA (Food)·F-0681-2023·2023-04-05

    Seasoned Green Laver Recalled for Undeclared Soy, Wheat, Fish, and Sesame

    Lemonland Food Corp is recalling Seasoned Green Laver sold in Washington due to undeclared allergens including soybean, wheat, fish (anchovy), and sesame seeds. Consumers with allergies to these ingredients should not consume this product.

    Product
    Seasoned Green Laver distributed in un-labeled plastic containers 8oz. and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0667-2023·2023-04-05

    Seasoned Perilla Leaves Recalled Due to Undeclared Allergens

    Lemonland Food Corp recalled Seasoned Perilla Leaves in 6oz, 8oz, and 12oz containers distributed in Washington because the product contains undeclared allergens: sesame, soy, wheat, fish, and shrimp.

    Product
    Seasoned Perilla Leaves distributed in un-labeled plastic containers 6oz, 8oz, and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0481-2023·2023-04-05

    FDA Recalls Glimepiride Tablets Due to Manufacturing Quality Violations

    Direct Rx is voluntarily recalling Glimepiride 2 mg tablets nationwide due to manufacturing practice violations. The recall affects multiple lot numbers of 30-count and 90-count bottles distributed across the United States.

    Product
    Glimepiride, USP, 2 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0488-30; b) 90-count bottle, NDC 61919-0448-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0682-2023·2023-04-05

    Hot Pepper in Soy Sauce Recalled for Undeclared Soy and Wheat

    Lemonland Food Corp recalled Hot Pepper in Soy Sauce distributed in 12-ounce containers due to undeclared soybean and wheat allergens. Consumers with soy or wheat allergies should not consume this product.

    Product
    Hot Pepper in Soy Sauce distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0672-2023·2023-04-05

    Seasoned Garlic Stem Recalled Due to Undeclared Fish and Sesame Allergens

    Lemonland Food Corp recalled Seasoned Garlic Stem products due to undeclared fish (anchovy) and sesame allergens. Affected products were distributed in Washington from February 16-23, 2023.

    Product
    Seasoned Garlic Stem distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0659-2023·2023-04-05

    Spicy Cucumber Salad recalled for undeclared sesame, fish, and wheat allergens

    Lemonland Food Corp recalls Spicy Cucumber Salad due to undeclared sesame seeds, fish (anchovy), and wheat allergens. The product was distributed in multiple container sizes in Washington.

    Product
    Spicy Cucumber Salad distributed in un-labeled plastic containers 8oz, 12oz. and 16oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0663-2023·2023-04-05

    Seasoned Hot Pepper Leaves recalled for undeclared fish and sesame allergens

    Lemonland Food Corp recalls Seasoned Hot Pepper Leaves from Washington due to undeclared Fish (Anchovy) and Sesame Seeds allergens. Consumers with allergies to these ingredients should not consume the product.

    Product
    Seasoned Hot Pepper Leaves distributed in un-labeled plastic containers 8oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0665-2023·2023-04-05

    Stir-Fried Kimchi Recalled for Undeclared Allergens: Fish, Shrimp, Wheat, Sesame

    Lemonland Food Corp recalls 12 oz. containers of Stir-Fried Kimchi distributed in Washington due to undeclared allergens: fish (anchovy), shrimp, wheat, and sesame. Consumers with allergies to these ingredients should not consume this product.

    Product
    Stir-Fried Kimchi distributed in un-labeled plastic containers 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1303-2023·2023-04-05

    Express Mini 500 Chest Drain Recalled for Inadequate Instructions

    The Express Mini 500 Dry Seal Chest Drain has been recalled because its instructions do not adequately warn against draining it for continued use or using it outside healthcare settings. Approximately 8,184 cases were distributed worldwide.

    Product
    Express Mini 500 Dry Seal Chest Drain, Part Number 16400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V240000·2023-04-05

    MCI Recalls 2019-2021 Coaches Due to Obstructed Rear Lighting

    Motor Coach Industries is recalling 2019-2021 J4500, D45CRTLE, and J3500 coaches because rear lighting may be obstructed by bike racks, increasing crash risk.

    Product
    MCI — MCI D45CRTLE, J4500, J3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0664-2023·2023-04-05

    Seasoned Vegetables Recalled for Undeclared Soy and Wheat Allergens

    Lemonland Food Corp is recalling Seasoned Vegetables (Cirsium Setidens) distributed in Washington due to undeclared soy and wheat allergens. Consumers with soy or wheat allergies should not consume this product.

    Product
    Seasoned Vegetables (Cirsium Setidens) distributed in un-labeled plastic containers 6oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0662-2023·2023-04-05

    Seasoned Korean Lettuce Recalled for Undeclared Fish Allergen

    Lemonland Food Corp recalled Seasoned Korean Lettuce distributed in Washington due to undeclared fish (anchovy). Consumers with fish allergies should not consume this product.

    Product
    Seasoned Korean Lettuce distributed in un-labeled plastic containers 6oz or 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1306-2023·2023-04-05

    FDA recalls ACL ELITE refurbished analyzer to remove Anti-Xa test

    Instrumentation Laboratory recalled ACL ELITE refurbished coagulation analyzers to remove the HemosIL Liquid Anti-Xa test definition.

    Product
    ACL ELITE Refurbished-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0000880311R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0685-2023·2023-04-05

    Stainless Steel Water Bottles Recalled for Lead Leaching from Welded Screw Cap

    BINDLE BOTTLE is recalling Stainless Steel Water Bottles because the cup's screw cap is attached by a weld that leaches lead into drinking water.

    Product
    Stainless Steel Water Bottle The product comes in four sizes: 32 oz., 24 oz., 20 oz., and 13 oz.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1295-2023·2023-04-05

    PCRopsis BCSNano nucleic acid extraction kit recalled for misleading label statements

    Entopsis, Inc. is recalling PCRopsis BCSNano nucleic acid extraction kits due to misleading statements on the product label. The affected lot (Lot 3, expiring 11/2023) was distributed nationwide and internationally.

    Product
    PCRopsis BCSNano (1mL), REF 2276001; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0486-2023·2023-04-05

    Simvastatin Tablets Recalled Nationwide Over Manufacturing Practice Deviations

    Direct Rx is recalling 269 bottles of Simvastatin 40 mg nationwide due to Good Manufacturing Practice deviations. No adverse events have been reported. Consult your healthcare provider before changing your medication.

    Product
    Simvastatin, USP, 40 mg, Rx Only, Packaged as a 90-count bottle, NDC 61919-0431-90, Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1307-2023·2023-04-05

    ACL ELITE PRO analyzer test definition removal for Anti-Xa reagent

    Instrumentation Laboratory is removing test definitions for HemosIL Liquid Anti-Xa reagent from ACL Elite and Elite Pro analyzers with Serial Number 16053360R and prior. The recall affects 33 units distributed worldwide.

    Product
    ACL ELITE PRO Refurbished)-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0001000311R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0666-2023·2023-04-05

    Seasoned Garlic with Salt and Vinegar recalled for ingredient statement update

    Lemonland Food Corp recalled seasoned garlic distributed in Washington after providing consignees with an updated ingredients statement.

    Product
    Seasoned Garlic with Salt and Vinegar distributed in un-labeled plastic containers 6oz, 8oz, and 12oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0482-2023·2023-04-05

    Glimepiride tablet recall due to manufacturing practice deviations

    Direct Rx is recalling Glimepiride 4 mg tablets nationwide due to manufacturing process deviations. The recall is voluntary and affects specific lots of 30-count and 90-count bottles.

    Product
    Glimepiride, USP, 4 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0250-30; b) 90-count bottle, NDC 61919-0250-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0484-2023·2023-04-05

    Drug Manufacturer Recalls Simvastatin Tablets for Manufacturing Deviations

    Direct Rx recalled Simvastatin 10 mg tablets nationwide due to manufacturing process deviations discovered during production. No illnesses or injuries have been reported.

    Product
    Simvastatin, USP, 10 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0688-30 b) 90-count bottle, NDC61919-0688-90, Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0476-2023·2023-04-05

    Drug Recall: Montelukast Sodium Tablets Due to Manufacturing Deviations

    Direct Rx is recalling Montelukast Sodium 10 mg tablets nationwide due to manufacturing process deviations. The voluntary recall affects approximately 508 bottles distributed across the United States.

    Product
    Montelukast Sodium Tablets, USP, 10 mg Tablets, Rx Only, Packaged as: a) 30-count bottle, NDC 61919-0009-30; b) 90-count bottle, NDC 61919-0009-90; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1299-2023·2023-04-05

    PCR Reagent Recalled for Misleading Label Statements

    Entopsis, Inc. is recalling 397 units of PCRopsis Reagent RVD with RVD Enhancer due to misleading label statements. The affected products were distributed nationwide and internationally.

    Product
    PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL, VALIDATION USE ONLY, REF 78336001; b) 25 mL, REF 78336025; c) 100 mL, REF 78336100; Extraction-free PCR from saliva, urine, &swab specimens in transport medium, nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1297-2023·2023-04-05

    PCRopsis Activator nucleic acid extraction kits recalled for misleading labels

    Entopsis, Inc. is recalling PCRopsis Activator nucleic acid extraction kits due to misleading label statements. The products were distributed nationwide and internationally.

    Product
    PCRopsis Activator: a) 1.5mL, REF 228001; b) 0.5mL,REF 228002; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0478-2023·2023-04-05

    Prescription Drug Ropinirole 0.25 mg Tablets Recalled for Manufacturing Deviations

    Direct Rx is recalling Ropinirole, USP, 0.25 mg tablets (NDC 72189-0364-30, Lot 21JU2210) nationwide due to Good Manufacturing Practice (cGMP) deviations. The firm voluntarily initiated this recall on March 13, 2023.

    Product
    Ropinirole, USP, 0.25 mg Tablets, Rx Only, Packaged as a 30-count bottle, NDC 72189-0364-30; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0480-2023·2023-04-05

    Drug Recall: Glimepiride Tablets Due to Manufacturing Deviations

    Direct Rx is recalling Glimepiride, USP, 1 mg Tablets nationwide due to cGMP deviations. The firm-initiated recall impacts both 30-count and 90-count bottles distributed across the USA.

    Product
    Glimepiride, USP, 1 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0723-30; b) 90-count bottle, NDC 61919-0723-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide