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 deaths or serious injuries are reported, 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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21901–21925 of 26035

  • HighNHTSA·22V270000·2022-04-22

    2022 Alliance RV Paradigm Recreational Trailers Recalled for LP Gas Leak

    Alliance RV is recalling certain 2022 Paradigm, Avenue, and Valor recreational trailers due to cracked quick disconnect fittings in the LP gas system that can cause gas leaks, creating a fire hazard.

    Product
    ALLIANCE RV — 2022 ALLIANCE RV PARADIGM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22125·2022-04-21

    Insignia Air Fryers and Air Fryer Ovens Recalled for Fire and Burn Hazards

    About 635,000 Insignia air fryers and air fryer ovens can overheat, posing fire and burn hazards. Best Buy is offering refunds or store credit for affected units sold between November 2018 and February 2022.

    Product
    Insignia Air Fryers and Air Fryer Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22124·2022-04-21

    Children's Pajamas Recalled Due to Flammability Hazard

    The Red League is recalling approximately 910 children's pajamas that fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries. Consumers should remove the pajamas from children and contact The Red League for return instructions and a full refund.

    Product
    Children's pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22123·2022-04-21

    LUXE+WILLOW Heated Blankets Recalled Due to Fire and Burn Hazards

    MWA LLC is recalling about 4,200 LUXE+WILLOW heated blankets sold nationwide from January to March 2022 because the blanket can overheat if left plugged in and powered on for extended periods, creating fire and burn hazards.

    Product
    LUXE+WILLOW Heated Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22741·2022-04-21

    Monti Kids Wooden Push Toys Recalled Due to Choking Hazard

    Monti Kids is recalling about 1,375 Wooden Push Toys because the rolling cylinder can separate, exposing internal balls that pose a choking hazard to children. No injuries have been reported.

    Product
    Monti Kids Wooden Push Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22742·2022-04-21

    Overhead Garage Storage Racks Recalled for Impact Injury Hazard

    SafeRacks/Monsterrax overhead garage storage racks may collapse from the ceiling due to defective hex bolts, posing an impact injury hazard. About 12,800 units sold online from September through December 2021.

    Product
    Overhead Garage Storage Racks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0918-2022·2022-04-20

    Cub 2 Enclosed Bed Canopy System Recalled Due to Potential Misuse

    Sensory Medical Inc recalled 225 units of the Cub 2 Enclosed Bed Canopy System for potential misuse risk. The firm is updating product warnings and precautions for devices distributed before December 16, 2021.

    Product
    Cub 2 Enclosed Bed Canopy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0998-2022·2022-04-20

    Giant Eagle Happy Face Cookies recalled for undeclared milk allergen

    Giant Eagle is recalling Happy Face Cookie 4-packs due to undeclared milk allergen. Consumers with milk allergies should avoid this product.

    Product
    Giant Eagle, Happy Face Cookie 4 Pack 25051900000, 11 oz, Clam Shell
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1005-2022·2022-04-20

    Back to Nature Cheese Crackers Recalled Due to Undeclared Egg and Milk Allergens

    B&G Foods is recalling Back to Nature Cheddalicious Cheese Flavored Crackers due to undeclared egg and milk allergens caused by mispackaging. Consumers with egg or milk allergies should discard the product or return it.

    Product
    Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0999-2022·2022-04-20

    Giant Eagle Happy Face Cookies Recalled for Undeclared Milk Allergen

    Giant Eagle recalled Happy Face Cookies from two Ohio stores due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Giant Eagle, Happy Face Cookie Single 25065900000
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0765-2022·2022-04-20

    FDA Recalls IDArubicin Injection for Particulate Matter Contamination

    Teva Pharmaceuticals is recalling IDArubicin Hydrochloride Injection vials due to the presence of silica and iron oxide particulate matter. The recall affects nationwide distribution within the United States.

    Product
    IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use, 5mL Single Dose Vial, Rx Only, Teva Pharmaceuticals, USA, Inc., North Wales, PA 19454, NDC 0703-4154-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0931-2022·2022-04-20

    Siemens Atellica CH Lithium reagent recalled for potential reagent carryover

    Siemens Healthcare Diagnostics recalls approximately 2,158 units of Atellica CH Lithium_2 reagent (Lot Numbers 110108, 110185, 110238, 110302) due to potential for reagent carryover affecting quality control results, patient samples, and calibrator results.

    Product
    Atellica CH Lithium_2 (LITH_2), Siemens Material Number 11097637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0928-2022·2022-04-20

    Siemens Atellica CH Calcium_2 Reagent Carryover Recall

    Siemens is recalling Atellica CH Calcium_2 diagnostic reagent due to potential reagent carryover that could impact quality control, patient samples, and calibrator results. The recall affects approximately 2,395 units distributed globally and in the US.

    Product
    Atellica CH Calcium_2 (CA_2), Siemens Material Number 11097644
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0922-2022·2022-04-20

    FDA Recalls Abbott Vascular Priority Pack Accessory Kits for Leak and Connection Issues

    Abbott Vascular is recalling 23 lots of Priority Pack accessory kits and packs due to reports of leaks and loose connections in the devices.

    Product
    20/30 Priority Pack Accessory Kit/.096 RHV - REF 1000186 WPL2122270-01 (2019-03-01) 20/30 Priority Pack w/.115 RHV - REF 1000186-115 WPL2122270-02 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0872-2022·2022-04-20

    Conductivity Sensors in Dialog Hemodialysis Systems May Crack and Leak

    B Braun Medical Inc is recalling conductivity sensors used in Dialog and Dialog+ hemodialysis systems due to potential cracks that could cause dialysate circuit leaks, affecting ultrafiltration during treatment.

    Product
    Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems. Conductivity Sensor (BIC) - VERSION 2, Article Code Number 3456102A. These conductivity sensors may be used as spare parts for the following dialysis machines: 710200L (UDI 04046963686345), 710200S (UDI 0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0995-2022·2022-04-20

    Skippy Reduced Fat Peanut Butter recalled for potential steel contamination

    Skippy Reduced Fat Creamy Peanut Butter (40 oz) is being recalled due to potential steel contamination. No illnesses have been reported.

    Product
    SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label.; SKIPPY Reduced Fat Creamy Peanut Butter NET WT 40 oz. (2 LB 8 OZ) 1.13 kg UPC 037600105200 packaged in clear plastic jar with blue label and
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0994-2022·2022-04-20

    Wilton Cookie Bunny Hutch Kit Recalled for Missing Milk Allergen

    Wilton Industries is recalling specific lots of Chocolate Cookie Bunny Hutch Kit because milk is not listed in the allergen statement, despite being present in the product.

    Product
    Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, total weight 28.7oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0920-2022·2022-04-20

    Verigene Processor SP Recalled for No Call Results

    Luminex Corporation is recalling 4 Verigene Processor SP diagnostic devices that repeatedly failed to produce results, returning No Call outputs instead. Two of three customer complaints involved this malfunction.

    Product
    Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0924-2022·2022-04-20

    Abbott INDEFLATOR Plus 30 Device Recalled for Leaks and Connection Faults

    Abbott Vascular is recalling INDEFLATOR Plus 30 balloon inflators due to increasing complaints of leaks and intermittent loose connections that could affect device function during medical procedures.

    Product
    INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0942-2022·2022-04-20

    ARIA Radiation Therapy Management Software May Cause Treatment Location Error

    Varian ARIA radiation therapy management software versions 13.6 through 16.1 may generate incorrect treatment plan values that could direct radiation therapy to the wrong location. No illnesses have been reported.

    Product
    ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0989-2022·2022-04-20

    Cinnamon Crumb Cake Recalled for Potential Foreign Materials

    Continental Mills voluntarily recalls Krusteaz Cinnamon Crumb Cake (Lot KX2063) due to potential foreign materials that could pose a choking or injury risk.

    Product
    Item # 722-0105, Krusteaz Cinnamon Crumb Cake. Product is shelf stable and packaged in a box. net wt. 21 oz., UPC 0 41449 11140 7.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0996-2022·2022-04-20

    SKIPPY Reduced Fat Chunky Peanut Butter recalled for potential steel contamination

    Skippy Foods recalls SKIPPY Reduced Fat Chunky Peanut Butter due to potential small steel contaminants. The recall affects 9,353 cases distributed across multiple U.S. states.

    Product
    SKIPPY Reduced Fat Chunky Peanut Butter NET WT 16.3 oz (1 LB 3 OZ) 462 g UPC 037600104999 packaged in clear plastic jar with blue label
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-0993-2022·2022-04-20

    Taylor Farms Thai Noodle Salad Kit Recalled for Plexiglass Contamination

    Taylor Farms is recalling Thai Noodle Salad Kit (108 oz) due to plexiglass found in an ingredient. The affected product was distributed to Kroger locations in Illinois, Indiana, Kentucky, Missouri, and Ohio with best by dates March 10-16, 2022.

    Product
    Taylor Farms - Thai Noodle Salad Kit packaged in 108oz plastic bag *Product packages all salad ingredients separate then ships to retail location. Deli counter at retail location mix ingredients and sale as per order servings.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0921-2022·2022-04-20

    Abbott Vascular 20/30 Indeflator Recalled for Leaks and Connection Failures

    Abbott Vascular recalls 20/30 Indeflator medical devices due to increased complaints of leaks and loose connections. The recall affects 17 product lots distributed nationwide and internationally.

    Product
    20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0991-2022·2022-04-20

    Fish Breader Recalled Nationwide for Foreign Material Contamination

    Continental Mills is recalling Gordon Choice Southern Style Fish Breader (Lot KX2065) nationwide due to the presence of foreign materials. Consumers should not consume this product and should return it to the place of purchase.

    Product
    Item # 744-4930, Gordon Choice Southern Style Fish Breader. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 93901 75622 0.
    Category
    Food
    Distribution
    Distributed nationwide