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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

1626–1650 of 5642

  • SevereFDA (Food)·F-0919-2024·2024-02-07

    Queso Fresco from Multiple Brands Recalled for Listeria Contamination

    Rizo Lopez Foods, Inc. is recalling various queso fresco products from multiple brands due to potential Listeria monocytogenes contamination. The affected products were distributed to retail locations in multiple U.S. states.

    Product
    Tio Francisco, El Huache, La Ordena Fresco (Michoacano) Available to consumers at retail deli counters in various sizes Tio Francisco, San Carlos Available to consumers at retail deli counters in various sizes Rizo Bros. Queso 8 oz. UPC 7-27242-00159-5 Don Francisco 10 oz. UP
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-0805-2024·2024-02-07

    Multiple Tuna Products Recalled Due to Listeria Monocytogenes Contamination

    Ocean Group Inc. is recalling tuna products distributed in California due to potential Listeria monocytogenes contamination identified through FDA environmental sampling.

    Product
    201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRESH, WILD Y/F,B/E #2 GRADE 201300 TUNA BLUEFIN SPAIN SPA F LB 201301 TUNA BLUEFIN SPAIN (SE) SPAIN F LB 201304 TUNA BLUEFIN SPAIN G&G SPAIN F LB 201508 TUNA BLUE FIN GG JAPAN FR JPN F LB 201900 TU
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0917-2024·2024-02-07

    Cheese product recalled for Listeria monocytogenes contamination

    Rizo Lopez Foods is recalling Tio Francisco Blanco Suave cheese due to potential Listeria monocytogenes contamination. Affected products have date codes through March 23, 2024.

    Product
    Tio Francisco Blanco Suave 14 oz. UPC 7-27242-05355-6
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-0925-2024·2024-02-07

    Ricotta cheese products recalled for Listeria monocytogenes contamination

    Multiple ricotta cheese products from Rizo Lopez Foods are recalled nationwide due to potential Listeria monocytogenes contamination. Affected batches have best-by dates through April 2, 2024.

    Product
    365 Whole Foods Market Ricotta Part Skim 15 oz. UPC 9-94824-63052 365 Whole Foods Market Ricotta Whole Milk 15 oz. UPC 9-94824-96245 Ricotta Part Skim 65%, 70%, 75% Moisture (bulk)
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Devices)·Z-0775-2024·2024-02-07

    FDA recalls EVair 03 compressor models for elevated formaldehyde levels

    FDA recalls EVair 03 air compressors (models 1609000, 1609002) for elevated formaldehyde when used with certain ventilators. The hazard was identified during preliminary testing under worst-case conditions: elevated room temperature (40°C) and minimal gas flow (2 L/min).

    Product
    EVair 03 (Jun-air) air compressor, model numbers: 1609000 and 1609002
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0278-2024·2024-02-07

    FentaNYL Citrate IV Bags Recalled Due to Double-Dose Filling System Malfunction

    FentaNYL citrate intravenous bags are recalled nationwide because a semi-automated filling system can malfunction and deliver double the intended dose. Patients and healthcare providers should immediately quarantine affected lots.

    Product
    FentaNYL citrate PF, 2500 mcg per 250 mL 0.9% Sodium Chloride (10 mcg per mL), Item F3342, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-072-82.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0863-2024·2024-02-07

    Smiths Medical Medfusion Model 3500 Syringe Pump Software Defects

    Smiths Medical recalls Medfusion Model 3500 syringe pumps (software versions before v6.0.0) due to multiple programming defects that could affect medication delivery rates, timing, and accuracy.

    Product
    smiths medical Medfusion Model 3500 Syringe pump
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·24V499000·2024-02-07

    2023-2024 Fisker Ocean recalled for sudden loss of drive power

    A battery management system failure in 2023-2024 Fisker Ocean vehicles can cause sudden loss of drive power. Fisker will replace the affected pumps at no cost.

    Product
    FISKER — 2024 FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0864-2024·2024-02-07

    Smiths Medical Medfusion 4000 Syringe Pump Software Defects Recall

    The FDA is recalling Smiths Medical Medfusion Model 4000 syringe pumps due to software defects affecting medication delivery, alarms, and display accuracy. Users should install the latest software version to correct these issues.

    Product
    smiths medical Medfusion Model 4000 syringe pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0942-2024·2024-02-07

    EZDilate Wire Guided Balloon Recalled for Device Malfunction and Patient Injury Risk

    Olympus recalled 3,767 EZDilate Wire Guided Balloons due to reported inflation, deflation, and retrieval problems causing bursting, leaking, and foreign body lodgement in patients. The devices dilate strictures in the alimentary tract.

    Product
    EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-1555
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V245000·2024-02-04

    2021 Jayco Redhawk motorhomes recalled for power steering connection defect

    Certain 2021 Jayco Redhawk motorhomes have a defective power steering connection that can cause sudden loss of power steering and brake assist, increasing crash risk. Dealers will replace the defective parts free of charge.

    Product
    JAYCO — 2021 JAYCO REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V079000·2024-02-02

    2022-2023 BMW IX and X1 driver airbag may fail to deploy in crash

    Certain 2022 and 2023 BMW IX and X1 vehicles have defective driver-side airbags that may not deploy during a crash. Dealers will replace the airbags at no charge.

    Product
    BMW — 2023 BMW IX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24097·2024-02-01

    DailySale Magnetic DIY Balls Magic Cube Recalled for Ingestion Hazard

    DailySale Inc. is recalling its 216-piece 5mm Magnetic DIY Balls Magic Cube because the high-powered magnets violate federal toy safety regulations. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Magnetic DIY Balls Magic Cube, 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24096·2024-02-01

    Fishing Games Recalled for High-Powered Magnet Ingestion Hazard

    Huihuang Trading is recalling Fishing Games sold on Amazon.com from June through July 2023 because they contain magnets that exceed federal safety limits. Swallowed magnets can become lodged in the digestive system and cause serious injury or death.

    Product
    Fishing Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24107·2024-02-01

    BISSELL Multi Reach Hand and Floor Vacuum Cleaners Recalled for Fire Hazard

    BISSELL is recalling about 142,000 Multi Reach Hand and Floor Vacuum Cleaners because the battery pack can overheat and smoke, creating a fire risk. Six reports included the battery catching fire, causing minor property damage and burn injuries in some cases.

    Product
    BISSELL® brand Multi Reach Hand and Floor Vacuum Cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0782-2024·2024-01-31

    Publix Custom Burrito Bowls Recalled Due to Listeria Contamination Risk

    Publix Super Markets is recalling Custom Burrito Bowls due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient. The bowls were distributed in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia during December 5-14, 2023.

    Product
    Publix Custom Burrito Bowls, variable weights and sizes, packed in plastic containers, intended for immediate consumption.
    Category
    Food
    Distribution
    8 states
  • CriticalFDA (Food)·F-0775-2024·2024-01-31

    Tapee Tea packets recalled for undeclared pharmaceutical contamination

    Tapee Tea packaged in paper packets is being recalled because samples contain undeclared pharmaceutical substances (dexamethasone and piroxicam). The contamination poses serious health risks from unintended medication exposure.

    Product
    Tapee Tea packaged in paper packets - 5 packets per bag
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0781-2024·2024-01-31

    Publix Custom Made Pizzas Recalled Due to Listeria Contamination in Lettuce

    Publix Custom Made Pizzas distributed in eight states are being recalled because the shredded lettuce ingredient may contain Listeria monocytogenes.

    Product
    Publix Custom Made Pizzas, variable weights and sizes, packed in cardboard box, intended for immediate consumption.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0261-2024·2024-01-31

    Drug recall: Bleomycin injection vials recalled due to glass contamination

    Pfizer is recalling 3,546 vials of Bleomycin for Injection due to the presence of glass particulate matter. The affected lot was distributed nationwide in the USA, Netherlands, and Libya.

    Product
    BLEOMYCIN — BLEOMYCIN (BLEOMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0789-2024·2024-01-31

    Pan Surtido Bakery Products Recalled for Undeclared Allergens

    Lara's Bakery 3 LLC is recalling Pan Surtido multi-pack bakery trays distributed in Iowa and Wisconsin through November 2023 due to undeclared allergens including sesame, coconut, soy, and milk, with potential for wheat and eggs.

    Product
    Pan Surtido with label reading: Panaderia Lara's Bakery, 701 N 3rd Ave Suite C Marshalltown IA 50158. Multi-pack tray containing Concha, Cema, Polvoron, Tostado de Guatemala, Pan de Guatemala, Canasta, Garibaldi, Marianas, Muffin, Pan Fino, Pastel Glass, Pan de Trigo, Puerco, Bol
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0784-2024·2024-01-31

    Publix Custom Made Platters Recalled Due to Potential Listeria Contamination

    Publix is recalling custom made platters distributed across eight states due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient. Consumers should not eat platters prepared between December 5-14, 2023.

    Product
    Publix Custom Made Platters, variable weights and sizes, packed in plastic containers, intended for immediate consumption (https://www.publix.com/mc/order-ahead/order-deli-platters?nav=header).
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0777-2024·2024-01-31

    Outrageous Oat Cookies Recalled for Undeclared Wheat Allergen

    Wegmans Food Markets is recalling Outrageous Oat Cookies due to undeclared wheat. The product poses a serious health risk to consumers with wheat allergies or celiac disease.

    Product
    Outrageous Oat Cookies packaged in 5pk and also sold in Bulk
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0780-2024·2024-01-31

    Publix Sub Sandwiches Recalled for Potential Listeria Contamination

    Publix Custom Made Sub Sandwiches are being recalled due to potential Listeria monocytogenes contamination in the shredded lettuce ingredient supplied by Fresh Express. Products were distributed between December 5-14, 2023 in southeastern states.

    Product
    Publix Custom Made Sub Sandwiches, variable weights and sizes, individually wrapped in paper, intended for immediate consumption (https://www.publix.com/menu-subs-and-wraps?merch=hp_viz_nav_subs_wraps).
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0317-2024·2024-01-31

    Robitussin Honey CF Max Nighttime Adult Recalled for Microbial Contamination

    Haleon US Holdings LLC is recalling Robitussin Honey CF Max Nighttime Adult cough medicine due to microbial contamination. The FDA Class I recall affects 21,900 bottles distributed nationwide.

    Product
    Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg, Diphenhydramine HCl 25mg), 8 FL OZ (237 mL) bottle, Distributed by: GSK Consumer Healthcare, Warren, NJ 07059
    Category
    Drug
    Distribution
    Distributed nationwide