The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

18251–18275 of 50406

  • 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
  • HighFDA (Devices)·Z-0475-2022·2022-01-19

    CT Scanner Software Update Causes Head Image Quality Degradation

    Siemens SOMATOM Definition Edge CT scanners with software version VB20_SP5 may produce degraded head images, increasing the risk of patient misdiagnosis. Devices have been distributed nationwide.

    Product
    SOMATOM Definition Edge -Computed tomography system Model 10590000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0495-2022·2022-01-19

    LigaSure Blunt Tip Laparoscopic Sealer Devices Recalled for Jaw Opening Defect

    Covidien is recalling LigaSure Blunt Tip Laparoscopic Sealer/Divider devices (lot 11320187X) due to an assembly defect that may prevent the device jaws from opening after tissue application, creating a risk of bleeding and tissue injury.

    Product
    LigaSure Blunt Tip Laparoscopic Sealer/Divider, Nano-Coated, Product Number LF1837
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0504-2022·2022-01-19

    Everything Swapples Recalled for Potential Plastic Contamination

    SWAP FOODS LLC is recalling Everything Swapples (11.14 oz) due to an ingredient that may be contaminated with small pieces of plastic. Affected product was distributed to retail stores in Pennsylvania and Wisconsin.

    Product
    Everything Swapples, Net Wt. 11.14 OZ, UPC 8 64390 00021 3
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0488-2022·2022-01-19

    Orthopaedic Stem Implants Recalled for Undersized Bore Manufacturing Defect

    DePuy Orthopaedics is recalling approximately 870 GLOBAL UNITE STD STEM implants worldwide because an undersized spigot bore may prevent proper separation, causing potential surgical delay or bone damage.

    Product
    GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0473-2022·2022-01-19

    CT Scanner Software Defect May Degrade Image Quality

    Software version VB20_SP5 in certain Siemens CT scanners may degrade head image quality, increasing misdiagnosis risk. The recall affects 794 units distributed nationwide.

    Product
    SOMATOM Definition AS-Computed tomography system Model 8098027
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0390-2022·2022-01-19

    Local Fixe LLC Frozen Dinner Rolls Wheat Allergen Not Declared

    Local Fixe LLC is recalling frozen dinner rolls because wheat is not declared on the label, even though flour (which contains wheat) is listed as an ingredient. This poses a serious risk to consumers with wheat allergies.

    Product
    Dinner Rolls are shaped in rounds and sold frozen. Packaged in clear plastic Ziploc style plastic bags. The weight per package s 1.323 lbs/600 grams. The label is read in parts: "***Dinner rolls ***Flour, sourdough starter, water, egg, sugar, salt, grape seed oil, active dry…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0399-2022·2022-01-19

    Raw Vegan Protein Peanut Butter Recalled for Undeclared Coconut

    NutraCap Labs LLC is recalling Raw Vegan Protein Peanut Butter dietary supplement because it contains undeclared coconut, which poses a risk to consumers with coconut allergies.

    Product
    RAW VEGAN PROTEIN PEANUT BUTTER NET WEIGHT 2.04LBS (925 GRAMS) DIETARY SUPPLEMENT Other Ingredients: Pea Protein Isolate, Brown Rice Protein, ***Sunflower (Non-Dairy) Creamer, Salt, Steviol Glycoside (95%) Manufactured in the U.S.A. for RAW, 838 SW Federal Highway, Stuart…
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0465-2022·2022-01-19

    Subdermal Needle Electrode Corkscrew Recall: Risk of Blue Hub Detachment

    Technomed Europe is recalling 117,672 disposable subdermal needle electrodes due to risk of the blue hub detaching, potentially leaving the needle in the patient's scalp.

    Product
    Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C, TE/S50725-001C, and TE/S50715-001.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0378-2022·2022-01-19

    Bosket Bread Jalapeño Cheese Bread Recall: Undeclared Allergens

    Bosket Bread Company is recalling Jalapeño Cheese Bread sold in Washington because the packaging lacks an ingredient statement, leaving major allergens (wheat, milk, egg, soy, sesame) undeclared.

    Product
    Jalape¿o Cheese 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-0371-2022·2022-01-19

    Bosket Bread Ciabatta Loaves Recalled for Undeclared Allergens

    Bosket Bread Company is recalling Ciabatta Loaves sold in Washington because the packages lack ingredient statements, leaving wheat, milk, egg, soy, and sesame undeclared. Consumers with allergies to these ingredients face a health risk.

    Product
    Ciabatta Loaves, 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-0487-2022·2022-01-19

    Orthopaedic Implant Stems Recalled for Undersized Spigot Bore Defect

    DePuy Orthopaedics is recalling GLOBAL UNITE REV STEM SZ 10 implants because the spigot bore may be undersized, preventing proper separation of components during revision surgery and potentially causing bone damage.

    Product
    GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600
    Category
    Medical Device
    Distribution
    Distributed nationwide