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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8951–8975 of 113902

  • SevereFDA (Food)·F-0900-2025·2025-06-11

    Fresh Take Crave Away Turkey Cheese Croissant Recall Due to Listeria

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Turkey & Cheese Croissant sandwiches because Listeria monocytogenes was detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh Take Crave Away Turkey & Cheese Croissant; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58552 0
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0910-2025·2025-06-11

    Fresh Take Tuna Mac Pasta Recalled for Listeria Contamination Risk

    Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Mike's Tuna Mac Pasta (9.5oz containers, Best By dates 05/09/2025–05/19/2025) because Listeria monocytogenes was detected on food contact surfaces at the manufacturer's facility.

    Product
    Fresh Take Crave Away Mike's Tuna Mac Pasta; 9.5oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58560 5
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0853-2025·2025-06-11

    Fresh & Ready Foods Ham & Cheese Dark Wheat Sandwich recall

    Fresh & Ready Foods is recalling Ham & Cheese Dark Wheat Sandwiches because Listeria monocytogenes was detected on food contact surfaces in the manufacturing facility.

    Product
    Fresh & Ready Foods Ham & Cheese Dark Wheat Sandwich, 7oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89294 3
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1809-2025·2025-06-11

    Medline Surgical Kits with Codman Disposable Perforator recalled

    Medline surgical kits containing Codman Disposable Perforators are being recalled because certain lots have inadequate welds that may cause the perforator to break or separate during use.

    Product
    Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS983611N 3. CRANIOTOMY CDS, SKU CDS983467J 4. CRANIOTOMY PACK, SKU DYNJ85807A, DYNJ85927 5. MAJOR CRANIOTOMY PACK, SKU DYNJ82007A
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Food)·H-0003-2025·2025-06-11

    Fresh Cut Cucumber Slices Marketside Recalled for Salmonella Risk

    Walmart's Marketside fresh cut cucumber slices are recalled due to potential Salmonella contamination. The recall affects 522 units sold at 12 retail locations in Texas.

    Product
    Fresh cut cucumber slices, Marketside, packaged in clear plastic circular container with clear plastic lid and white adhesive label with black print, Walmart, Inc. Bentonville, AR 72716
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1810-2025·2025-06-11

    Medline Craniotomy Kits with Defective Codman Disposable Perforators

    Medline is recalling craniotomy kits containing Codman Disposable Perforators with inadequate welds that may break or separate during use.

    Product
    Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-1896-2025·2025-06-11

    Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall

    Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.

    Product
    Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1895-2025·2025-06-11

    Signature Laparoscopic Debakey Grasper Instruments Recalled for Insulation Defect

    Silex Medical is recalling 8 units of Signature Laparoscopic Debakey Grasper instruments (Model 5862100) due to incomplete insulation on the shaft near the rotator wheel, which could expose the user or patient to electrical contact.

    Product
    Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1893-2025·2025-06-11

    Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect

    Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0838-2025·2025-06-11

    Pecan Caramel Bars Recalled for Undeclared Allergen Labels

    New Grains Gluten Free Bakery is recalling Pecan Caramel Bars sold in Utah because printing quality issues made allergen declarations for egg, milk, and pecans unreadable or missing on the package.

    Product
    Pecan Caramel Bars Individually wrapped in plastic. Ingredients: White rice flour, Sugar, Honey, Pecan pieces, Butter, Eggs, Rice milk, Potato flour, Vanilla, Baking powder, Xanthan gum, Unflavored gelatin, Sea salt Contains: Egg, Milk, Tree nuts
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0455-2025·2025-06-11

    Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination

    Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2025·2025-06-11

    Luminex VERIGENE Gram Negative Blood Culture Test Recalled

    Luminex is recalling VERIGENE Gram Negative Blood Culture test cartridges due to a consumable issue that may produce incorrect results on a small portion of one lot.

    Product
    VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test, REF 20-006-021; for use with the sample-to-results VERIGENE System; invitro diagnostic test
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0928-2025·2025-06-11

    GNC Women's 30+ Vitapak recalled due to undeclared fish allergen

    GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.

    Product
    GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
    Category
    Food
    Distribution
    48 states
  • HighFDA (Food)·H-0008-2025·2025-06-11

    Bengal King Family Pack Vegetable Singara Contains Undeclared Peanut

    South Asian Food Inc. is recalling Bengal King Family Pack Vegetable Singara due to undeclared peanut, a major allergen that poses a serious risk to consumers with peanut allergies.

    Product
    Bengal King Family Pack Vegetable Singara
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·H-0002-2025·2025-06-11

    Bedner Growers cucumbers recalled for potential Salmonella contamination

    Bedner Growers, Inc. is recalling cucumbers shipped from May 3–12, 2025, due to potential Salmonella contamination. Affected products were distributed in Florida in cardboard boxes of 24, 36, or 68 count.

    Product
    Cucumbers, Wholesale Produce Supply, Bedner Growers, Inc. 10066 Lee Road Boynton Beach, FL 33473 (561)733-5490. Cucumbers were packaged in cardboard shipping boxes to customers with packaging sizes consisting of 68, 36, or 24 count per box.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1911-2025·2025-06-11

    Olympus EVIS EXERA III Duodenovideoscope TJF-Q190V Contamination Risk

    Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.

    Product
    Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0837-2025·2025-06-11

    Dye-Free Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Dye-Free Frosted Sugar Cookies due to printing quality issues that failed to clearly declare allergens (egg, milk, soy) on the label. The product was distributed in Utah.

    Product
    Dye-Free Frosted Sugar Cookie: Gluten-free dye-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1900-2025·2025-06-11

    Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall

    Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.

    Product
    Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0823-2025·2025-06-11

    Artisan Multigrain Bread recalled for undeclared egg allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling Artisan Multigrain Bread (32 oz packages) distributed in Utah because label printing quality failed to clearly declare the egg allergen present in the product.

    Product
    Artisan Multigrain Bread: Gluten-free multigrain bread, vacuum-sealed clear plastic, 32 oz, 1 loaf/package Ingredients: White rice flour, Water, Egg whites, Tapioca flour, Honey, Golden flax seed, Palm oil, Potato flour, Yeast, Sugar, Psyllium husk powder, Rice bran, Sea salt,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1885-2025·2025-06-11

    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical US LLC is recalling Palindrome Precision Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. Affected units were distributed worldwide including the US, Canada, and Mexico.

    Product
    Palindrome Precision Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1886-2025·2025-06-11

    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled

    Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.

    Product
    Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0832-2025·2025-06-11

    Frosted Sugar Cookies Recalled for Undeclared Allergens

    New Grains Gluten Free Bakery is recalling Frosted Sugar Cookies because the label does not clearly declare allergens: Egg, Milk, and Soy. The product was distributed in Utah.

    Product
    Frosted Sugar Cookie: Gluten-free frosted sugar cookies, clear plastic bag, 4 oz, 6 cookies/package Ingredients: White rice flour, Powdered sugar, Butter, Sugar, Palm shortening, Sprinkles, Rice milk, Egg whites, Potato flour, Imitation vanilla, Baking powder, Xanthan gum, Gela
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0828-2025·2025-06-11

    Gluten-Free Cinnamon Raisin Bagels Recalled for Undeclared Egg Allergen

    NEW GRAINS GLUTEN FREE BAKERY is recalling Cinnamon Raisin Bagels (16 oz, 4-count packages) due to poor label printing that fails to clearly declare the presence of egg allergen.

    Product
    Cinnamon Raisin Bagels: Gluten-free cinnamon raisin bagels, clear plastic bag, 16 oz, 4 bagels/package Ingredients: White rice flour, Water, Egg whites, Raisins, Honey, Tapioca flour, Golden flax seed, Palm fruit oil, Potato flour, Yeast, Sugar, Cinnamon, Psyllium husk powder,
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1889-2025·2025-06-11

    MAHURKAR Chronic Hemodialysis Catheter recalled for sterile barrier defect

    Mozarc Medical is recalling MAHURKAR Chronic Hemodialysis Catheter Sport Pack units due to a potential breach in sterile barrier packaging that could compromise the product's sterility.

    Product
    MAHURKAR Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1894-2025·2025-06-11

    Signature Laparoscopic Allis Clamp Grasper with Rotating Shaft Recalled

    Silex Medical is recalling the Signature Laparoscopic Instruments Allis Clamp Grasper due to incomplete insulation on the shaft, leaving an exposed area that could pose an electrical hazard during surgical procedures.

    Product
    Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5862030.
    Category
    Medical Device
    Distribution
    Distributed nationwide