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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27326–27350 of 90165

  • HighFDA (Food)·F-0389-2022·2022-01-19

    Pie Dough Recall: Undeclared Wheat Allergen

    Local Fixe LLC is recalling frozen pie dough products because wheat is not declared on the label, even though flour—which contains wheat—is an ingredient. The recall affects 181 packages distributed in Oregon.

    Product
    Pie Dough are packaged two crusts per pack and sold frozen. They are wrapped in white butcher paper. The weight per package is 1.257 lbs/540 grams. The label is read in parts: "***Pie Dough*** Flour, Butter (cream, milk, salt), Organic Palm Shortening, water, salt…
    Category
    Food
    Distribution
    1 state
  • HighCPSC·22054·2022-01-19

    FRIGG Silicone Pacifiers Recalled Due to Choking Hazard

    Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.

    Product
    FRIGG Silicone Pacifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0395-2022·2022-01-19

    Vemondo Vegan Dessert Cones Recalled for Undeclared Milk Allergen

    Lidl US Operations is recalling Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones because they contain undeclared milk, posing a risk to consumers with milk allergies.

    Product
    Vemondo Vegan Caramel & Pannacotta Non-Dairy Dessert Cones. 4-3.7 fl oz (110 mL) UPC 4 056489 468653
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0477-2022·2022-01-19

    OCT-Camera Laser Shut-Off Malfunction Poses Patient Safety Risk

    Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.

    Product
    OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22055·2022-01-19

    Children's Sleepwear Recalled for Flammability Standards Violation

    Childrensalon is recalling about 180 children's sleepwear garments that fail to meet U.S. flammability standards, posing a burn injury risk. Consumers should stop using the garments immediately and contact Childrensalon for return instructions.

    Product
    Children's Sleepwear Garments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0369-2022·2022-01-19

    Bosket Bread Sourdough Dinner Rolls Lack Required Ingredient Labels

    Bosket Bread Company is recalling Sourdough Dinner Rolls distributed in Washington because the products lack ingredient statements, leaving consumers unable to identify undeclared wheat, milk, egg, soy, or sesame allergens.

    Product
    Sourdough Dinner Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0388-2022·2022-01-19

    Fresh Flour Tortillas Recalled for Undeclared Wheat Allergen

    Local Fixe LLC is recalling Fresh Flour Tortillas because wheat is not declared on the label, even though flour (a wheat product) is listed as an ingredient. This poses a risk to consumers with wheat allergies.

    Product
    Fresh Flour Tortillas are packaged in a clear Ziploc style plastic bag. The weight per package is 1.323 lbs/600 grams. The label is read in parts: "***Fresh Flour Tortillas ***Flour, water, organic palm shortening, salt, baking powder*** ww.localfixe.com***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0380-2022·2022-01-19

    Bosket Bread Sesame Buns Recalled for Undeclared Allergens

    Bosket Bread Company is recalling Sesame Buns (1–1.5 lbs) distributed in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Sesame Buns, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0472-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality Nationwide

    Siemens SOMATOM Confidence CT scanners with software version VB20_SP5 may experience degraded head image quality, creating a potential risk of misdiagnosis. The recall affects 108 units distributed nationwide.

    Product
    SOMATOM Confidence -Computed tomography systems Model 10590100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0492-2022·2022-01-19

    Flat Panel Detector May Display Abnormal Images During Surgical Procedures

    Canon Medical's flat panel detectors used in Alphenix surgical systems may display abnormal horizontal stripes and fail to recover by restarting, potentially causing operators to work without proper visual guidance during procedures.

    Product
    Flat Panel Detector, Model Number: TFP-800A, used with the Alphenix Systems, Item Numbers: INFX-8000V, INFX-8000C, INFX-8000F, and INFX-8000H.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0484-2022·2022-01-19

    GLOBAL UNITE STD STEM orthopedic implant manufacturing defect recall

    DePuy Orthopaedics is recalling GLOBAL UNITE STD STEM orthopedic implants due to undersized spigot bore diameter that may prevent proper removal during revision surgery, risking surgical delay and bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0379-2022·2022-01-19

    Bosket Bread Olive Bread recalled for undeclared allergens

    Bosket Bread Company is recalling Olive Bread (Kalamata olives) products distributed in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Olive Bread (Kalamata olives), Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0370-2022·2022-01-19

    Bosket Bread Rosemary Bread recalled for undeclared allergens

    Bosket Bread Company is recalling Rosemary Bread products sold in Washington due to missing ingredient statements, which fail to declare potential wheat, milk, egg, soy, or sesame allergens.

    Product
    Rosemary Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0377-2022·2022-01-19

    Bosket Bread Hot Dog Buns Recalled for Undeclared Allergens

    Bosket Bread Company is recalling Hot Dog Buns distributed in Washington because the products lack ingredient statements on the package, leaving wheat, milk, egg, soy, and sesame allergens undeclared.

    Product
    Hot Dog Buns, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0372-2022·2022-01-19

    Nitroglycerin Lingual Spray Recalled for Defective Delivery System

    Padagis US LLC is recalling Nitroglycerin Lingual Spray due to a defective delivery system that may prevent proper medication administration. The recall affects 11,868 bottles distributed nationwide.

    Product
    NITROGLYCERIN LINGUAL — NITROGLYCERIN LINGUAL (NITROGLYCERIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0485-2022·2022-01-19

    DePuy Joint Stem May Have Undersized Bore, Complicating Surgical Removal

    DePuy Orthopaedics has recalled 3 units of GLOBAL UNITE REV STEM SZ 8 due to an undersized spigot bore. Separation of the implant components may not be possible without surgical delay and/or bone damage.

    Product
    GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0362-2022·2022-01-19

    Metoprolol Tartrate Tablets Recalled for Foreign Metal in Tablets

    Rubicon Research Private Limited is recalling Metoprolol Tartrate 25 mg tablets (batch #210211H1, expiration February 2024) due to a complaint of metal embedded in a tablet.

    Product
    METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0486-2022·2022-01-19

    Hip stem implants recalled due to undersized bore defect

    DePuy Orthopaedics is recalling 781 hip stem implants that may have an undersized spigot bore diameter, potentially preventing surgical removal without additional surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0393-2022·2022-01-19

    Squid Ink Fettuccine Pasta Recall: Undeclared Wheat Allergen

    Local Fixe LLC is recalling Squid Ink Fettuccine fresh pasta because wheat is not declared on the label, despite flour being an ingredient. The product poses a risk to consumers with wheat allergies.

    Product
    Squid Ink- Fettucine is raw fresh pasta portioned into 4 ounce portions. Each portion is rolled in a wax deli sheet and bulk packaged into a reusable plastic container with varying weight. Each container will have 40-60 portions, net wt. 10-15 lbs (4.536-6.804 kg). The label…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0375-2022·2022-01-19

    Bosket Bread Brioche Dinner Rolls recalled for undeclared allergens

    Bosket Bread Company is recalling Brioche Dinner Rolls because the packages lack ingredient statements, leaving consumers unaware of potential allergen contents including wheat, milk, egg, soy, or sesame.

    Product
    Brioche Dinner Rolls, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0367-2022·2022-01-19

    Bosket Bread 8 Grain Bread recalled for undeclared allergens

    Bosket Bread Company is recalling 8 Grain Bread products sold in Washington because packages lack ingredient statements, leaving common allergens (wheat, milk, egg, soy, and sesame) undeclared.

    Product
    8 Grain Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0483-2022·2022-01-19

    Hip Stem Component Recalled Due to Undersized Bore Diameter

    DePuy is recalling GLOBAL UNITE STD STEM SZ 6 orthopedic stems due to undersized spigot bore that may prevent safe removal during revision surgery, risking surgical delays and bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0376-2022·2022-01-19

    Bosket Bread English Muffin Bread Recalled for Missing Ingredient Labels

    Bosket Bread Company is recalling English Muffin Bread products distributed in Washington because packages lack ingredient statements, leaving consumers unable to identify potential allergens including wheat, milk, egg, soy, or sesame.

    Product
    English Muffin Bread, Bosket Bread brand. The Net weight of the products range from 1-1.5 lbs. No UPC. Product is packaged in food grade plastic bag with the black Bosket Bread logo sticker on the front, but without the ingredients statement affixed on a package.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0479-2022·2022-01-19

    Radiotherapy Planning Software BeamAdjust and VeriSoft Recalled for Measurement Errors

    PTW North America is recalling BeamAdjust 2.2 and VeriSoft 8.0 software due to measurement errors that can report incorrect radiation doses in patient treatment plans.

    Product
    Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S080032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0478-2022·2022-01-19

    OCT Camera Laser Safety Shut-Off Malfunction Affects Three Units

    Haag-Streit USA is recalling OCT-Camera 211 01 A3 units due to malfunction of the automatic laser beam shut-off. The device may not correctly recognize when the laser beam is safely switched off.

    Product
    OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4
    Category
    Medical Device
    Distribution
    Distributed nationwide