The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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20201–20225 of 90018

  • HighFDA (Devices)·Z-1300-2023·2023-04-05

    PCRopsis Reagent RVD-RT in vitro diagnostic kit recall for misleading labels

    Entopsis, Inc. is recalling PCRopsis Reagent RVD-RT diagnostic kits due to misleading label statements that could affect proper use and test interpretation.

    Product
    PCRopsis Reagent RVD-RT, IVD: a) 1 mL, REF 78378001; b) 25 mL, REF 78378025; c) 100 mL, REF 78378100; Extraction-free PCR at room temperature; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0687-2023·2023-04-05

    Almost Famous Popcorn Poppy Chow recalled for undeclared peanut allergen

    Rieckhoff Family Businesses is recalling Almost Famous Popcorn Poppy Chow because peanuts are listed in ingredients but omitted from the allergen statement. Consumers with peanut allergies may be at serious risk.

    Product
    Almost Famous Popcorn Poppy Chow, 9.9 oz bag (UPC 8 5001151513)
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0668-2023·2023-04-05

    Seasoned Vegetable Recalled for Undeclared Wheat, Fish, and Sesame

    Lemonland Food Corp recalled Seasoned Vegetable (Deodeok) distributed in Washington due to undeclared allergens: wheat, fish (anchovy), and sesame seeds. Consumers with allergies to these ingredients should not consume the product.

    Product
    Seasoned Vegetable (Deodeok) 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 (Drugs)·D-0487-2023·2023-04-05

    Apollo Care Fentanyl and Ropivacaine Epidural Injection Recalled for Contamination

    Apollo Care is recalling 215 bags of Fentanyl and Ropivacaine epidural injection (Lot AC-016581) due to suspected microbial growth on external packaging. The recall affects product distributed in Missouri.

    Product
    Fentanyl 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (1mg/mL) added to 250mL 0.9% Sodium Chloride, For Epidural Use Only, Rx only, 3801 Mojave Ct. Suite 101, Columbia, MO 65202, NDC 71170-950-25
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-0669-2023·2023-04-05

    Perilla Leaves in Soybean Paste recalled for undeclared allergens

    Lemonland Food Corp recalls Perilla Leaves in Soybean Paste for undeclared soybean, wheat, fish, and shrimp allergens. Consumers with these allergies should avoid the product.

    Product
    Perilla Leaves in Soybean Paste 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-1290-2023·2023-04-05

    GaGa Pro Class IV Laser Projectors Recalled for FDA Compliance Failure

    GaGa Pro Lighting Equipment Co. manufactures Class IV Laser Light Show projectors that are being recalled due to non-compliance with FDA's Performance Standard for laser products. Eleven units distributed nationwide are affected.

    Product
    GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2023·2023-04-05

    Covidien Shiley Lo-Pro Tracheal Tube Cuffed Recalled for Potential Inflation System Leaks

    Covidien is recalling Shiley Lo-Pro Oral/Nasal Tracheal Tubes due to potential leaks in the inflation system. The affected devices, used during anesthesia and procedures, may not maintain proper airway sealing.

    Product
    COVIDIEN Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed REF 86051 7.0 mm I.D. The Shiley Lo-Pro Oral/Nasal Tracheal Tube Cuffed are indicated for airway management by oral/nasal intubation of the trachea for anesthesia or other short-term procedures.
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Drugs)·D-0534-2023·2023-04-05

    Prescription Drug Dabigatran Etexilate Recalled for Excess Nitrosamine Impurity

    Ascend Laboratories is recalling 12,804 bottles of Dabigatran Etexilate 150mg capsules nationwide due to detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake limit caused by manufacturing process deviations.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1293-2023·2023-04-05

    Surgical Robot Instrument Carriage Loose Due to Manufacturing Defect

    Intuitive Surgical is recalling da Vinci Xi and da Vinci X surgical systems because the instrument carriage can become loose due to a manufacturing defect in the linear rail component.

    Product
    da Vinci Xi Surgical System Model IS4000 da Vinci X Surgical System Model IS4200
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1316-2023·2023-04-05

    Baxter Automated Peritoneal Dialysis System Electrical Safety Testing Failure

    Baxter Healthcare Corporation is recalling 16 Automated Peritoneal Dialysis Systems due to incomplete electrical safety testing. Affected devices require additional testing.

    Product
    Automated Peritoneal Dialysis System. Used for automatic control of dialysis solution exchanges.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-0661-2023·2023-04-05

    Seasoned Nut Recalled for Undeclared Peanut and Walnut Allergens

    Lemonland Food Corp recalled seasoned nut products for undeclared peanut and walnut allergens. Consumers with allergies to these nuts should not consume affected products sold in Washington between February 16-23, 2023.

    Product
    Seasoned Nut 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-0683-2023·2023-04-05

    Seasoned Seaweed Recalled for Undeclared Sesame and Wheat Allergens

    Lemonland Food Corp is recalling Seasoned Seaweed distributed in Washington due to undeclared sesame seeds and wheat. Consumers with these allergies should not consume the product.

    Product
    Seasoned Seaweed 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-0678-2023·2023-04-05

    Seasoned Lotus Root Recalled for Undeclared Soybean and Wheat

    Lemonland Food Corp recalled Seasoned Lotus Root for containing undeclared soybean and wheat allergens. Consumers with allergies to these allergens should not consume the product.

    Product
    Seasoned Lotus Root 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 (Drugs)·D-0479-2023·2023-04-05

    Ropinirole 1 mg Tablets Recalled Nationwide for Manufacturing Process Deviations

    Direct Rx is recalling Ropinirole 1 mg tablets nationwide due to manufacturing process deviations. Consult a pharmacist before stopping this medication.

    Product
    Ropinirole, USP, 1 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
  • HighFDA (Food)·F-0658-2023·2023-04-05

    Stir-Fried Fish Cake Recalled Due to Undeclared Allergens

    Lemonland Food Corp recalled stir-fried fish cake due to undeclared soybean, wheat, fish, and sesame allergens. The affected products were distributed in Washington from February 16 to 23, 2023.

    Product
    Stir-Fried Fish Cake distributed in un-labeled plastic containers 6oz, 8oz, 12oz, and 16oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1311-2023·2023-04-05

    Fluoroscopic X-Ray System Recalled for Unintended Table Movement Risk

    Siemens ARTIS pheno X-ray systems may experience unintended table movement that the system fails to detect, risking injury to patients, staff, or operators. The FDA is recalling 141 affected units nationwide.

    Product
    ARTIS pheno systems with a Siemens Healthineers table or a Trumpf/ MAQUET table-A Fluoroscopic X-Ray system. Material # 10849000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0675-2023·2023-04-05

    Seasoned Dried Pollack Recalled for Undeclared Allergens

    Lemonland Food Corp is recalling Seasoned Dried Pollack distributed in Washington for undeclared Fish, Wheat, and Soybean allergens. Consumers with these allergies should not consume this product.

    Product
    Seasoned Dried Pollack distributed in un-labeled plastic containers 6oz., 8 oz., and 12 oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0670-2023·2023-04-05

    Seasoned Peanut Recalled Due to Undeclared Peanut, Soybean, Wheat, and Sesame

    Lemonland Food Corp is recalling Seasoned Peanut distributed in Washington due to undeclared allergens including peanut, soybean, wheat, and sesame seeds. Containers were labeled at H-mart, G-mart, and M2M retail stores.

    Product
    Seasoned Peanut 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 (Devices)·Z-1304-2023·2023-04-05

    ACL Elite Analyzer HemosIL Liquid Anti-Xa test definition removal

    Instrumentation Laboratory is removing the HemosIL Liquid Anti-Xa test definition from ACL Elite/Elite Pro Analyzers. This affects 358 units in the US and 558 units internationally.

    Product
    ACL ELITE- Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0000880311
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0680-2023·2023-04-05

    Stir-Fried Dried Squid Recalled for Undeclared Milk, Wheat, and Soybean

    Lemonland Food Corp recalled Stir-Fried Dried Squid distributed in Washington for undeclared Milk, Wheat, and Soybean allergens. Consumers with allergies to these allergens should not consume the product.

    Product
    Stir-Fried Dried Squid 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 (Devices)·Z-1309-2023·2023-04-05

    Leksell Stereotactic System Recall: Incorrect Instructions Distributed with Devices

    Elekta Instrument AB is recalling 70 Leksell Stereotactic System neurosurgical devices due to incorrect Instructions for Use being distributed with the devices. Incorrect documentation for neurosurgical equipment could impact proper device use.

    Product
    Instructions for Use for the following Leksell Stereotactic System and Leksell Neurosurgical Instruments: (1) Part #A2800-26, Backlund Catheter Insertion Needle Kit III; (2) Part #A2800-15, Backlund Catheter Insertion Needle Kit I; (3) Part #A2600-01, Backlund Haematoma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1286-2023·2023-04-05

    CRP Immunoturbidimetric Reagent Recalled for Positive Bias in Patient Samples

    Randox Laboratories is recalling CRP Immunoturbidimetric reagent Batch 588434 because the antibody component shows a positive bias on patient samples, producing elevated test results compared to previous batches. Quality control samples remain within acceptable range.

    Product
    CRP Immunoturbidimetric reagent. Intended for the quantitative in vitro determination of CRP concentration in serum Catalogue number: CP3826
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0674-2023·2023-04-05

    Seasoned Radish Sliced Recalled for Undeclared Fish, Shrimp, and Sesame

    Lemonland Food Corp is recalling Seasoned Radish Sliced products distributed in Washington due to undeclared Fish, Crustacean, and Sesame allergens. Consumers with these allergies should not consume this product.

    Product
    Seasoned Radish Sliced distributed in un-labeled plastic containers 6oz., 8 oz., and 12 oz. Containers were then labeled at H-mart, G-mart, or M2M retail store.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0673-2023·2023-04-05

    Wild Leek Recalled for Undeclared Soy, Wheat, and Fish Allergens

    Lemonland Food Corp is recalling Wild Leek sold in Washington due to undeclared allergens: soybean, wheat, and fish (anchovy). Consumers with allergies to these ingredients should avoid this product.

    Product
    Wild Leek 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 (Devices)·Z-1302-2023·2023-04-05

    Chest Drain Valve Recalled for Insufficient Safety Instructions

    The Atrium Pneumostat Chest Drain Valve has been recalled because its instructions lack sufficient precautions against improper drainage and use outside healthcare settings.

    Product
    Atrium Pneumostat Chest Drain Valve, Part Number 16100
    Category
    Medical Device
    Distribution
    Distributed nationwide