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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2651–2675 of 7451

  • CriticalFDA (Food)·F-1632-2018·2018-07-11

    Caito Foods Recalls Mixed Melon for Potential Salmonella Contamination

    Caito Foods Service, Inc. is recalling mixed melon products due to potential Salmonella contamination. The recall covers specific Kroger brand fruit snack trays distributed in 23 states.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Kroger FRUIT SNACK TRAY 1/40Z, 40 oz., UPC: 826766140152, Clear Generic Label Distributed by Renaissance Food Group
    Category
    Food
    Distribution
    23 states
  • CriticalFDA (Food)·F-1640-2018·2018-07-11

    Caito Foods Recalls Mixed Melon for Potential Salmonella Contamination

    Caito Foods Service, Inc. is recalling multiple brands of mixed melon sold at Walmart due to potential Salmonella contamination.

    Product
    Multiple Brands Mixed Melon: Customer Product Description Pack Weight UPC Label Description/Brand Walmart FRUIT TRAY 2/48Z 48 oz., UPC: 681131180207 Freshness Guaranteed label
    Category
    Food
    Distribution
    23 states
  • CriticalNHTSA·18V452000·2018-07-06

    Nissan Recalls 2007-2008 Versa Models Due to Air Bag Inflator Defect

    Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·057-2018·2018-06-29

    L&D Market Recalls Wasabi Chicken Wraps for Undeclared Milk Allergen

    L&D Market Inc. is recalling wasabi chicken wraps due to misbranding and undeclared milk allergens. The products were shipped to retail locations in Cambridge, Massachusetts.

    Product
    L&D Market Inc. — L&D Market, Inc. Recalls Chicken Wrap Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-2253-2018·2018-06-27

    Draeger Apollo Anesthesia Machine Recalled for Potential Hypoxic Gas Delivery

    Draeger Medical is recalling 72 Apollo Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients, posing a risk of death.

    Product
    Apollo Anesthesia Machine; Cat. no. 8605310 Product Usage: Indicated as a continuous flow anesthesia system. The Apollo may be used for manually assisted or automatic ventilation, delivery of gases and anesthetic vapor, and monitoring of oxygen and CO2 concentration…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2251-2018·2018-06-27

    Draeger Fabius GS Tiro Anesthesia Machine Recalled for Hypoxia Risk

    Draeger Medical is recalling 31 Fabius GS Tiro anesthesia machines because a fault could allow 100% nitrous oxide delivery, creating a risk of hypoxic mixtures and patient death.

    Product
    Fabius GS Tiro Anesthesia Machine; Cat. no. 8606000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2252-2018·2018-06-27

    Draeger Fabius GS MRI Anesthesia Machine Recalled for Hypoxia Risk

    Draeger Medical is recalling four Fabius GS MRI Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients, potentially causing death.

    Product
    Fabius GS MRI Anesthesia Machine; Cat. no. 8607300 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2250-2018·2018-06-27

    Draeger Fabius GS Premium Anesthesia Machine Recalled for Hypoxia Risk

    Draeger Medical is recalling 62 Fabius GS Premium Anesthesia Machines because a fault could allow the device to deliver a hypoxic gas mixture to patients.

    Product
    Fabius GS Premium Anesthesia Machine; Cat. no. 8607000 Product Usage: Inhalation anesthesia machines for use in operating, induction and recovery rooms. They may be used with O2, N2O, and AIR supplied by a medical gas pipeline system or by externally mounted gas cylinders.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·051-2018·2018-06-20

    Texas Natural Meats Recalls Frozen Raw Ground Beef for E. coli O103

    Texas Natural Meats is recalling approximately 489 pounds of frozen raw ground beef products that may be contaminated with Shiga toxin-producing E. coli (STEC) O103.

    Product
    Texas Natural Meats — Texas Natural Meats Recalls Frozen Raw Ground Beef Products
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1546-2018·2018-06-20

    Pious Lion Pink Bali Product Recalled Due to Salmonella Contamination

    Pious Lion is recalling Pink Bali products in North Carolina and Tennessee after the North Carolina Dept. of Agriculture notified the firm that the product contains Salmonella.

    Product
    Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com
    Category
    Food
    Distribution
    2 states
  • CriticalNHTSA·18V402000·2018-06-15

    Mazda Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Mazda is recalling specific 2003-2011 models because passenger air bag inflators may explode during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, MPV, RX-8, MAZDASPEED6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V404000·2018-06-15

    Mazda Recalls MPV and RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2005-2006 MPV and 2005-2009 RX-8 vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA MPV, RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V403000·2018-06-15

    Mazda Recalls 2009-2010 RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2009-2010 RX-8 vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1536-2018·2018-06-13

    FDA Recalls Ethanol Extraction 190 Proof Grain Alcohol Due to Methanol Contamination

    Lake Michigan Distilling is recalling 190 Proof Non-Denatured Grain Alcohol due to methanol contamination that could cause serious injury or death if consumed.

    Product
    Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5 gals, 55 gallon drum, 8oz clear PVC cylinder bottles, all others heavy-duty polyethylene bottles (except single 55-gallon plastic drum).
    Category
    Food
    Distribution
    51 states
  • CriticalFDA (Food)·F-1595-2018·2018-06-13

    Melanie Mini Cookies with Caramel Flavor Recalled for Undeclared Peanuts

    Desly International Corp. is recalling Melanie Mini Cookies with Caramel Flavor because the products contain undeclared peanuts.

    Product
    Melanie Mini Cookies with Caramel Flavor in a 17.6 oz (500g) clear plastic package with UPC 4770049082126.
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Food)·F-1537-2018·2018-06-13

    Zoe's Cookies Vegan Tuxedo Fudge Recalled for Undeclared Walnuts

    Dough-To-Go Inc is recalling Zoe's Cookies Vegan Tuxedo Fudge because the product contains undeclared walnuts, a major food allergen.

    Product
    Zoe's Cookies Vegan Tuxedo Fudge, 4 oz. (153 kg) individually wrapped cookie. INGREDIENTS: UNBLEACHED FLOUR (WHEAT FLOUR, NIACIN, IRON, THIAMINE MONONITRATE, RIBOFLAVIN, ENZYME, FOLIC ACID), EVAPORATED CANE JUICE, VEGAN WHITE CHOCOLATE CHIPS (NON-BONE CHAR PROCESSED SUGAR…
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-1594-2018·2018-06-13

    Desly International Recalls Melanie Liubitelskie Cookies Due to Undeclared Peanuts

    Desly International Corp. is recalling Melanie Liubitelskie Cookies because they contain undeclared peanuts. The recall affects 250 cases distributed across 21 states.

    Product
    Melanie Liubitelskie Cookies in a 17.6 oz (500g) clear plastic package with UPC 4770049011188.
    Category
    Food
    Distribution
    21 states
  • CriticalFDA (Drugs)·D-0879-2018·2018-06-06

    Poseidon Platinum 4500 Recalled for Undeclared Sildenafil and Tadalafil

    Shoreside Enterprises Inc. is recalling Poseidon Xtreme PLATINUM 4500 because FDA analysis found undeclared sildenafil and tadalafil, making it an unapproved drug.

    Product
    POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0880-2018·2018-06-06

    FDA Recalls 7K Capsules Containing Undeclared Sildenafil and Tadalafil

    The FDA is recalling 7K capsules distributed by SX Power Co. because they contain undeclared sildenafil and tadalafil, making them unapproved drugs with unestablished safety and efficacy.

    Product
    7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0821-2018·2018-05-30

    FDA Recalls Rhino 69 Extreme 50000 for Undeclared Tadalafil

    The FDA is recalling Rhino 69 Extreme 50000 capsules because they contain undeclared tadalafil, an unapproved drug with unestablished safety and efficacy.

    Product
    Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack, Distributed by AMA Wholesale Inc. Chino Hills, CA, 91709-2618, UPC Code: 718122071128
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1485-2018·2018-05-23

    True Taste Seafood Hot Smoked Salmon Recalled for Botulism Risk

    True Taste, LLC. is recalling hot smoked salmon due to potential Clostridium botulinum contamination. The product was distributed in California and Illinois.

    Product
    True Taste Seafood Hot Smoked Salmon; Ingredients: salmon, salt, original smoke; To be weighed at point of sale - approximately 3/4 lb.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1457-2018·2018-05-23

    Whole Foods Recalls Explorateur French Triple Crème Cheese for Listeria Risk

    Whole Foods Market is recalling Explorateur French Triple Crème cheese due to potential Listeria monocytogenes contamination. The product was distributed in six states.

    Product
    Explorateur French Triple Cr¿me cheese (under the names Explorateur, Explorateur French Triple Cr¿me Cheese and Explorateur Triple Cr¿me French Cheese) which were both cut and packaged in clear plastic wrap, as well as sold in branded 8 oz. packages
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1484-2018·2018-05-23

    True Taste Hot Smoked Rainbow Trout Recalled for Botulism Risk

    True Taste, LLC. is recalling hot smoked rainbow trout in California and Illinois due to potential Clostridium botulinum contamination.

    Product
    True Taste Seafood Hot Smoked Rainbow Trout; Ingredients: rainbow trout, salt, original smoke; To be weighed at point of sale - approximately 3/4 lb.
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1483-2018·2018-05-23

    True Taste Cold Smoked Mackerel Recalled for Botulism Risk

    True Taste, LLC. is recalling Cold Smoked Mackerel due to potential Clostridium botulinum contamination. The product was distributed in California and Illinois.

    Product
    True Taste Seafood Cold Smoked Mackerel; Ingredients: Mackerel salt, original smoke; To be weighed at point of sale - approximately 3/4 lb.
    Category
    Food
    Distribution
    2 states