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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9476–9500 of 113902

  • HighFDA (Food)·F-0748-2025·2025-05-07

    Cookie Butter Banana Pie recalled for undeclared almond allergen

    Dianne's Fine Desserts is recalling Cookie Butter Banana Pie due to undeclared almonds. Consumers with almond allergies face risk of allergic reaction.

    Product
    Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained inside: "Cookie Butter Banana Pie" NET WT. 11 LB 2.8 OZ (5.06 kg) GROSS WT: 12.96 LB (5.88 kg)
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0741-2025·2025-05-07

    Ancient Grains Hoagie Roll recalled for glass fragment contamination

    Upper Crust Bakery LP is recalling Ancient Grains Hoagie Rolls due to glass fragments found on the product surface. The affected frozen rolls were distributed to six states.

    Product
    Ancient Grains Hoagie Roll, 4 oz, Paper carton (corrugated), CP45, Frozen
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0747-2025·2025-05-07

    Caraluzzi's Italian Style Seafood Burgers recalled for undeclared egg allergen

    Caraluzzi's Markets is recalling Italian Style Seafood Burgers because they contain undeclared egg, a major food allergen. Consumers with egg allergies who purchased these 8oz burgers should not eat them.

    Product
    Caraluzzi's Italian Style Seafood Burgers, 8oz; INGREDIENTS: Cod, Salmon, Shrimp, Scallops, Onions, Olive Oil, White Wine, Parsley, Sodium Caseinate (A Milk Derivative), Spices, Garlic, Salt, Paprika, Enzyme.; CONTAINS: Crustacean Shellfish, Fish, Milk; Distributed by Caraluzzi's
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1678-2025·2025-05-07

    Belmont 3.0 Liter Disposable Set Recalled for Cracked Female Connector

    Belmont Instrument LLC is recalling the 3.0 Liter Disposable Set (Model 903-00032) due to a potential crack in the female connector on the Heat Exchanger/patient line set that can cause fluid leaks during device priming.

    Product
    3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The P/N 903-00032 consists of 4 Large Volume Reservoirs (P/N 903-00018) and 4 Heat Exchanger/Patient Line set (P/N 403-00382). The two components are packaged separately in individual pouches and placed in the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2025·2025-05-07

    Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer Recall

    Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to incorrect sample barcode identification and processing errors that can result in erroneous and delayed test results.

    Product
    DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 Software versions: V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that meas
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2025·2025-05-07

    epoc BGEM BUN Test Cards for Blood Analysis System Recalled

    Siemens Healthcare Diagnostics is recalling epoc BGEM BUN Test Cards (25 pk) due to discrepant high pH results when samples are introduced with higher injection volumes on affected sensor configurations.

    Product
    epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515; epoc Software Version & Sensor Configuration: epoc Host SW v3.41.2, epoc NXS SW v4.14.9 & 4.14.11, Sensor Configuration 45.n.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V293000·2025-05-07

    2025 Polestar 3 vehicles recalled for faulty rearview camera display

    Polestar is recalling certain 2025 Polestar 3 vehicles because the rearview camera image may not display when the vehicle is in reverse, reducing driver visibility and increasing crash risk.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2025·2025-05-07

    Belmont Straight Inflow/Outflow Patient Line Kit recalled for potential connector crack

    Belmont Instrument LLC is recalling the Straight Inflow/Outflow Patient Line Kit (Model 902-00037) due to a potential crack in the female connector on the Heat Exchanger set that may cause fluid leaks during use.

    Product
    Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile, single-use, disposable set used with the Hyperthermia Pump. The Straight Inflow/Outflow Patient Line Kit (P/N 902-00037) consists of 4.4 Liter Reservoir (P/N 902-00034P), Heat Exchanger set (P/N 902
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2025·2025-05-07

    Stratus CS Acute Care cTNI TestPak cardiac troponin test recall

    Siemens Healthcare Diagnostics is recalling Stratus CS Acute Care cTNI TestPak, a cardiac troponin I test, due to an increased occurrence of false positive results during the product's shelf life.

    Product
    Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin I in heparinized plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0759-2025·2025-05-07

    Emily Kate's Gluten Free Vanilla Cake recalled for foil contamination

    Emily Kate's Foods is recalling Emily Kate's Gluten Free Vanilla Cake (6.4 oz) due to foil found in cake slices. The affected product was distributed to a consignee in Wisconsin.

    Product
    Emily Kate's Gluten Free Vanilla Cake, Net Wt. 6.4oz, Emily Kate's Foods, Kansas City, KS 66106, UPC 850581007253
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0750-2025·2025-05-07

    Dinstuhl's Peanut Brittle recalled for undeclared milk allergen

    Dinstuhl's Fine Candy Company is recalling Dinstuhl's Peanut Brittle (4 oz., UPC 7 68050 00205 3) because milk is not declared on the label, posing a risk to consumers with milk allergies.

    Product
    Dinstuhl's Peanut Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Corn Syrup, Baking Soda, Peanuts, Butter, Pure Vanilla Extract.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0751-2025·2025-05-07

    Dinstuhl's Pecan Brittle recalled for undeclared milk allergen

    Dinstuhl's Fine Candy Company is recalling Dinstuhl's Pecan Brittle (4 oz. bags) because the product contains milk that is not declared on the label, posing a risk to consumers with milk allergies.

    Product
    Dinstuhl's Pecan Brittle, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Pecans, Corn Syrup, Butter, Baking Soda, Salt, Vanilla.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0758-2025·2025-05-07

    La Victoria Cilantro Salsa recalled for wood pieces in ingredient

    La Victoria Cilantro Salsa (15.5 oz) is being recalled because the fresh cilantro ingredient may contain wood pieces. The product was distributed to California, Nevada, Oregon, Washington, and Michigan.

    Product
    La Victoria Cilantro Salsa; Med; Net Wt 15.5 OZ; UPC# 0 72101 34470 3; Distributed by: Megamex Foods, LLC Orange, CA 92868
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·25V294000·2025-05-07

    2022–2024 Audi Q5 Engine Cylinder Head Cover Screws Fire Risk

    Volkswagen Group of America (Audi) is recalling certain 2022–2024 Q5 and Q5 Sportback Quattro vehicles due to cylinder head cover screws that may loosen, causing oil leaks and increasing fire risk. Dealers will inspect and replace the screws at no charge.

    Product
    AUDI — AUDI Q5, Q5 SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V295000·2025-05-07

    2025 Freightliner trucks recalled for insufficient air tank capacity

    Daimler Trucks North America is recalling certain 2025 Freightliner, Western Star, and related models due to undersized air tanks that reduce braking performance and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, CASCADIA, BUSINESS CLASS M2, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0744-2025·2025-05-07

    Sundae Shoppe Cookies and Cream Mochi Ice Cream Recalled for Undeclared Wheat and Soy

    Gordon Desserts is recalling Sundae Shoppe Cookies and Cream Mochi Ice Cream due to undeclared wheat and soy allergens. The product was distributed to Connecticut, Virginia, Ohio, and Pennsylvania.

    Product
    Sundae Shoppe, Cookies and Cream Mochi Ice Cream, 6 count, 7.5 oz, Plastic sealed tray inside paper carton. 6 Pieces per carton, 8 cartons per shipper. Keep frozen.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1714-2025·2025-05-07

    Medline Sterile Water and Saline Bottles Leaking at Seal Interface

    Medline is recalling sterile water and 0.9% normal saline bottles due to leaking at the peel-foil and bottle opening interface. The defect affects 159 units distributed nationwide and internationally.

    Product
    Medline procedure kits, labeled as: HAND, REF DYNJ902002J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0745-2025·2025-05-07

    Multigrain Sourdough Bread Recalled for Potential Glass Foreign Material

    Giant Eagle, Inc. is recalling Multigrain Sourdough Freshly Baked and Half Multigrain Sourdough Artisan Bread due to potential glass contamination. The recall affects 240 cases distributed to PA, OH, MD, IN, and WV.

    Product
    Multigrain Sourdough Freshly Backed, and Half Multigrain Sourdough Artisan Bread, 15 oz; 7 oz, Bag, 1 unit
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0749-2025·2025-05-07

    Dinstuhl's Cashew Crunch Recalled for Undeclared Milk Allergen

    Dinstuhl's Fine Candy Company is recalling Dinstuhl's Cashew Crunch 4 oz. packages due to undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    Dinstuhl's Cashew Crunch, NET WT 4 oz. (113g), individually packaged in cellophane bags; Ingredients: Sugar, Cashews, Coconut, Corn Syrup, Brown Sugar, Butter, Salt, Baking Soda.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0746-2025·2025-05-07

    Chile Verde Egg Bites recalled for potential foreign material contamination

    Valley Fine Foods Co., Inc is recalling Chile Verde Egg Bites due to potential contamination with foreign materials. Affected products were distributed in Texas.

    Product
    CHILE VERDE EGG BITES; NET WT. 4.6 OZ (130 g); 2 egg bites/package
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0401-2025·2025-05-07

    Infuvite Adult Multiple Vitamins Injection Recalled Due to Cold Chain Failure

    Certain Infuvite Adult injectable vitamins were exposed to inadequate storage conditions after severe thunderstorms caused shipping delays exceeding 48 hours. The affected products' safety, quality, and potency may have been compromised.

    Product
    INFUVITE ADULT — INFUVITE ADULT (MULTIPLE VITAMINS INJECTION)
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0400-2025·2025-05-07

    Medroxyprogesterone Acetate Injectable Suspension Recalled Due to Cold Chain Disruption

    Medroxyprogesterone Acetate Injectable Suspension (150 mg/mL) distributed to medical facilities in Mississippi and Florida is recalled because severe thunderstorms caused shipping delays that may have compromised the product's storage conditions and safety.

    Product
    Medroxyprogesterone Acetate Injectable Suspension, USP, 150 mg / mL, 1 mL Single-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-0330-01
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0394-2025·2025-05-07

    Levothyroxine Sodium Tablets Recalled for Subpotency by Accord Healthcare

    Accord Healthcare is recalling 4,888 bottles of Levothyroxine Sodium Tablets (25 mcg) nationwide due to subpotency. The affected lot is D2300323 with expiration date 01/2026.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1707-2025·2025-05-07

    Medline procedure kits recalled for leaking sterile water and saline bottles

    Medline procedure kits containing sterile water and 0.9% normal saline bottles are being recalled because the bottles leak at the peel-foil and bottle opening interface. The kits were distributed worldwide including the US, Panama, and Canada.

    Product
    Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792
    Category
    Medical Device
    Distribution
    Distributed nationwide