The Recall Desk

State

Wyoming product recalls

72,820 recalls have nationwide distribution and so reach Wyoming. 3,219 additional recalls listed Wyoming specifically in their distribution scope.

What the numbers show

Total
3,219
Critical
762
Severe
543
Most recent
2026-09-02

Of the 3,219 recalls naming Wyoming we have scored against our rubric, 762 (24%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 543 (17%) are Severe.

These figures cover only the 3,219 recalls whose distribution notice names Wyoming specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

126–150 of 76039

  • SevereCPSC·26726·2026-08-27

    Walmart Recalls Mainstays Nine-Drawer Fabric Dressers Due to Tip-Over Risk

    Walmart is reannouncing a recall of Mainstays 9-Drawer Fabric Dressers because they pose tip-over and entrapment hazards that can cause serious injury or death to children.

    Product
    Mainstays 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26717·2026-08-27

    Conair Recalls Cuisinart Grill Brushes Due to Ingestion Hazard

    Conair is expanding a recall of over 3.6 million Cuisinart grill brushes because metal wire bristles can detach and be swallowed, posing a risk of serious internal injury.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V551000·2026-08-27

    Altec Recalls 2021-2023 Service Body Vehicles Due to Fire Risk

    Altec is recalling 2021-2023 Service Body vehicles because water leaks into strobe lights, causing electrical short-circuits that increase fire risk.

    Product
    ALTEC — ALTEC SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26719·2026-08-27

    HABA Rainbow Rattle Toy Recalled Due to Choking and Ingestion Hazards

    HABA USA is recalling Rainbow Rattle Grasping and Teething Toys because a glued knot can untie, exposing small parts that pose choking and ingestion risks to young children.

    Product
    HABA Rainbow Rattle Grasping and Teething Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26722·2026-08-27

    Excel Industries Recalls LED Light Kits for Ride-On Mowers Due to Fire Risk

    Excel Industries is recalling about 1,800 accessory LED light kits for Hustler and BigDog ride-on mowers because the light bars can overheat or produce flames.

    Product
    Accessory LED Light Kits used with certain ride-on mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26724·2026-08-27

    Little Loves & Co. Recalls Youth Clothing with Drawstrings

    Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.

    Product
    Little Loves & Co. Youth Clothing with Drawstrings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26718·2026-08-27

    MD Wipe Outz Numbing Tattoo Wipes Recalled for Child Poisoning Risk

    Diamond Wipes International is recalling MD Wipe Outz Numbing Tattoo Wipes because the packaging is not child-resistant, posing a risk of serious injury or death from child poisoning.

    Product
    MD Wipe Outz Numbing Tattoo Wipes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1242-2026·2026-08-26

    Coast Tropical Jalapeno Peppers Recalled for Potential Salmonella Javiana Contamination

    Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.

    Product
    Jalapeno Pepper packaged in bulk generic Coast Tropical cardboard packaging. Packaged in assorted bulk package sizes (10lbs, 40lbs, 35lbs, 20lbs, 38lbs 1 1/9 Bushel) ; Product of MX; Coast Tropical TX UPCs 73296608113; 73296600558; 73296610927; 73296600559; 732966107055; 02060042
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0788-2026·2026-08-26

    Fresenius Kabi Recalls Morphine Syringes Due to Labeling Error

    Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0801-2026·2026-08-26

    American Regent Recalls Tralement Injection Due to Particulate Matter

    American Regent is recalling 323,000 vials of Tralement (trace elements injection 4) due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    TRALEMENT — TRALEMENT (TRACE ELEMENTS INJECTION 4)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0802-2026·2026-08-26

    FDA Recalls Nicardipine Hydrochloride Injection Due to Particulate Matter

    American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NICARDIPINE HYDROCHLORIDE — NICARDIPINE HYDROCHLORIDE (NICARDIPINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2960-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Maxi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Maxi Speech Generating Device Model/Catalog Number: 1000799
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0797-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling Acetylcysteine Solution USP due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0793-2026·2026-08-26

    American Regent Recalls Cyanocobalamin Injections Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0794-2026·2026-08-26

    Aminocaproic Acid Injection Recalled for Particulate Matter Contamination

    American Regent, Inc. is recalling Aminocaproic Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    AMINOCAPROIC ACID — AMINOCAPROIC ACID (AMINOCAPROIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0791-2026·2026-08-26

    American Regent Recalls Nitroglycerin Injection Due to Particulate Matter

    American Regent, Inc. is recalling Nitroglycerin injection vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    NITROGLYCERIN — NITROGLYCERIN (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0795-2026·2026-08-26

    American Regent Recalls Atropine Sulfate Injection Due to Particulate Matter

    American Regent, Inc. is recalling Atropine Sulfate injection vials because they contain particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ATROPINE SULFATE — ATROPINE SULFATE (ATROPINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0764-2026·2026-08-26

    Shilpa Medicare Recalls Discolored Pemetrexed Injection Vials

    Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0796-2026·2026-08-26

    American Regent Recalls Acetylcysteine Solution Due to Particulate Matter

    American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.

    Product
    ACETYLCYSTEINE — ACETYLCYSTEINE (ACETYLCYSTEINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2959-2026·2026-08-26

    Tobii Dynavox Recalls TD Navio Midi Speech Generating Devices

    Tobii Dynavox is recalling TD Navio Midi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.

    Product
    TD Navio Midi Speech Generating Device Model/Catalog Number: 1000798
    Category
    Medical Device
    Distribution
    Distributed nationwide