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.

Filters

Agency

Category

Minimum severity

8801–8825 of 31219

  • ModerateFDA (Food)·F-0562-2025·2025-02-19

    Raspberry Jelly Sticks Dark recalled for undeclared Red #40 and Potassium Sorbate

    The Candy Basket Inc is recalling Raspberry Jelly Sticks DARK for undeclared Red #40 and Potassium Sorbate. A total of 516 four-pound bulk boxes were distributed in California, Oregon, and Washington.

    Product
    Raspberry Jelly Sticks DARK, Item Number CB747-D, packed and sold in bulk 4lbs. boxes. Product does not have a UPC and is not repackaged for retail. Product was sold out of bulk chocolate cases from candy stores to consumers without any labeling. Label on bulk 4lbs. box declar
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1125-2025·2025-02-19

    BD Pyxis MedStation 4000 Recalled for Drawer and Door Failures

    CareFusion 303, Inc. is recalling the BD Pyxis MedStation 4000 medication cabinet due to potential drawer and door failures that could delay access to stored medications.

    Product
    BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·25130·2025-02-13

    LoGest Climbing Ropes Recalled for Rope Breakage and Fall Hazard

    Setsmart is recalling LoGest Climbing Ropes sold on Amazon from March 2021 through November 2024 because the ropes can weaken and break, creating a fall hazard. One injury from a fall has been reported.

    Product
    LoGest Climbing Ropes with Carabiners and LoGest Climbing Ropes with Heavy-Duty Metal Hooks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25136·2025-02-13

    Igloo Rolling Coolers Recalled for Fingertip Amputation and Crushing Hazards

    Igloo is recalling approximately 1.06 million 90-quart rolling coolers because the tow handle can pinch fingertips against the cooler. The company has received 12 reports of fingertip injuries, including amputations and bone fractures.

    Product
    Igloo 90 Qt. Flip & Tow Rolling Coolers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25132·2025-02-13

    Portable Sleep Lamps Recalled Due to Lithium-Ion Battery Fire Hazard

    BlockBlueLight Multi-Mode Sleep Lamps are recalled because the lithium-ion battery can overheat while charging, creating fire and burn hazards. No injuries have been reported.

    Product
    Multi-Mode Sleep Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25131·2025-02-13

    SHEIN children's pajama sets recalled for flammability violation

    SHEIN Distribution Corporation recalls about 17,300 children's pajama sets sold on SHEIN.com between August 2023 and November 2024 for violating federal flammability standards for children's sleepwear, which poses a burn injury risk.

    Product
    SHEIN EVRYDAY Kids' Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25133·2025-02-13

    Spritz Resin Hanukkah Dino Menorahs Recalled Due to Fire Hazard

    About 4,400 Spritz Resin Hanukkah Dino Menorahs are recalled due to fire hazard. Target received 58 reports of the resin menorahs catching fire, scorching, charring, or melting when holding lit candles. No injuries reported. Return for full refund.

    Product
    Spritz Taper Resin Hanukkah Dino Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25135·2025-02-13

    AFTCO Youth Solitude Jackets Recalled for Strangulation Hazard

    AFTCO is recalling about 820 Youth Solitude Jackets due to a strangulation hazard from the retractable drawstring in the hood. The drawstring can get caught on objects, posing a risk of serious injury or death to children.

    Product
    Youth Solitude Jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0467-2025·2025-02-12

    Atkinson's Plain Hushpuppies Recalled Due to Undeclared Milk Allergen

    Atkinson Milling Company is recalling Atkinson's No Onions Plain Hushpuppies due to undeclared milk on the label. Consumers with milk allergies who consume this product risk allergic reaction.

    Product
    ATKINSON'S NO ONIONS PLAIN NO ONIONS HUSHPUPPIES NET WT. 2 LB. 8 OZ. UPC 0 72119 20304 7 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium Phosphate and Natural Flavors.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-1019-2025·2025-02-12

    Ivenix Infusion System software recalled for pump malfunction risk

    The FDA recalled Ivenix Infusion System software versions 5.9.2 and earlier for potential device malfunctions that could affect medication delivery. Two known anomalies may cause pump failure or improper infusion rates.

    Product
    Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care environments for the controlled administration of fluids through clinically accepted routes of administration.
    Category
    Medical Device
    Distribution
    15 states
  • SevereFDA (Food)·F-0532-2025·2025-02-12

    La Fiesta Bread Crumbs Recalled for Undeclared Sesame Allergen

    La Fiesta PAN RAYADO Bread Crumbs are being recalled for undeclared sesame, an allergen not listed on the label. The recall affects 2,200 cases distributed nationwide.

    Product
    La Fiesta PAN RAYADO Bread Crumbs, NET WT 8 OZ. (227g), UPC# 032327000886
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0462-2025·2025-02-12

    NuGo Dark Chocolate Chip Bars Recalled for Undeclared Milk

    Bazzini LLC is recalling NuGo Dark Chocolate Chip bars because they contain undeclared milk, which poses a health risk to consumers with milk allergies.

    Product
    NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0463-2025·2025-02-12

    NuGo Dark Pretzel Chocolate Chip Bars Recalled for Undeclared Milk

    Bazzini LLC is recalling NuGo Dark Pretzel/Chocolate Chip Multipack bars due to undeclared milk. The product poses a risk to consumers with milk allergies.

    Product
    NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct., 50g bar, 18 bars/tray, 9 trays/case. 40case/pallet
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0461-2025·2025-02-12

    NuGo Dark Chocolate Pretzel Bars Recalled for Undeclared Milk Allergen

    Bazzini LLC is recalling NuGo Dark Chocolate Pretzel bars because they contain undeclared milk. Consumers with milk allergies should not consume the affected product.

    Product
    NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark Chocolate / Vegan. 12g Protein
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0468-2025·2025-02-12

    VidaSlim Dietary Supplements Recalled for Toxic Yellow Oleander Presence

    VidaSlim dietary supplements and beverages are being recalled due to toxic yellow oleander contamination. The FDA Class I recall affects 760 units distributed nationwide.

    Product
    VidaSlim 90-day (Original Root, Root Plus, and Root Capsules), VidaSlim 30-day (Original Root, Root Plus, and Root Capsules), VidaSlim 7-day Sample Size (Original Root, Root Plus, and Root Capsules), and VidaSlim Hot Body Brew (Strawberry and Peach flavors),
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0466-2025·2025-02-12

    Atkinson's Hushpuppies Recalled Due to Undeclared Milk Allergen

    Atkinson Milling Company is recalling Atkinson's Hushpuppies with Onions due to undeclared milk. The product was not labeled as containing milk, posing a risk to consumers with milk allergies.

    Product
    ATKINSON'S HUSHPUPPIES WITH ONIONS NET WT. 1LB. (454 g) UPC 0 72119 20718 2 and NET WT. 2 LB. 8 OZ. UPC 0 72119 20305 4 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0464-2025·2025-02-12

    Pita bread recall due to undeclared milk allergen

    Cairo Bakery Pita Pocket Bread is recalled for containing undeclared milk. Packages with code 01/18 distributed in California may be affected.

    Product
    CAIRO BAKERY PITA POCKET BREAD TRADITIONAL RECIPE EXTRA LARGE 6 COUNT, NET WT. 16 OZ. (1 lb.) (454g)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0223-2025·2025-02-12

    Adrenalin Chloride Epinephrine Nasal Solution Recalled for Misleading Label

    Par Pharmaceutical is recalling Adrenalin Chloride Solution (Epinephrine Nasal Solution) due to a misleading label that resembles the FDA-approved Adrenalin epinephrine injection product, creating potential confusion.

    Product
    Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0533-2025·2025-02-12

    Seasoned Bread Crumbs Recalled Due to Undeclared Sesame Allergen

    La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.

    Product
    La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g), UPC# 032327000887
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0534-2025·2025-02-12

    Imported Prepared Monkfish Liver Recalled for Undeclared Milk Allergen

    Mutual Trading Company is recalling ANKIMOBO brand prepared monkfish liver (UPC: 72546611224) because the product contains an undeclared milk allergen. The product poses a risk to consumers with milk allergies.

    Product
    Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side contains English label that reads: #61122; ANKIMOBO (prepared Monkfish Liver) Ingredients: Monkfish Liver, Brewed Alcohol, (Rice, Rice Malt), Enzyme. CONTAINS:
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0530-2025·2025-02-12

    White Maeng da Kratom Powder Recalled for Possible Salmonella Contamination

    COREPACK MANUFACTURING INC is recalling White Maeng da kratom powder due to possible Salmonella contamination. The affected product was distributed throughout the United States.

    Product
    White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0524-2025·2025-02-12

    Donut Product Recalled for Potential Listeria Monocytogenes

    FGF, LLC is recalling approximately 2 million cases of its BAV CRM BAR DONUT product nationwide due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.

    Product
    item 8201923 BAV CRM BAR DONUT PFD 78 X 3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0526-2025·2025-02-12

    Apple Fritter Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling Apple Fritter Donuts (item 8201927) due to potential Listeria monocytogenes contamination. The recall affects 2,017,614 cases distributed nationwide in the US and Canada.

    Product
    item 8201927 APPLE FRITTER DONUT PFD 70 X 3.5OZ, NET WT 13.78 LB
    Category
    Food
    Distribution
    Distributed nationwide