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.

276–300 of 50462

  • HighFDA (Devices)·Z-3071-2026·2026-09-09

    Medline IV Start Kits Recalled Due to Potential Seal Defects

    Medline is recalling IV start kits containing BD ChloraPrep applicators with potentially open or incomplete seals, which may lead to infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators IV START KIT LAB DRAW-SH CDS860014Q IV START KIT DYKM1000B IV START KIT LAB DRAW-SH CDS860014P ULTRASOUND GUIDED PIV START KI DYNDV2684
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3076-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Applicator Seal Defects

    Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3049-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 4,636 convenience kits nationwide due to packaging wrinkles that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) CDS840396X, Catalog Number: CDS840396X; 2) CDS840396Y, Catalog Number: CDS840396Y; 3) CDS983348AA, Catalog Number: CDS983348AA; 4) CDS983348AB, Catalog Number: CDS983348AB; 5) CDS983672O, Catalog Number: CDS983672O; 6) CDS983672P, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1305-2026·2026-09-09

    Prince Bakery Recalls Italian and French Bread for Undeclared Sesame

    Prince Bakery Inc is recalling 150 units of Italian and French bread in New York because sesame is not declared in the ingredient statement.

    Product
    Prince ITALIAN BREAD; Sesame; ITALIAN & FRENCH BREAD, LARGE; NET WEIGHT 12 OZ. (340g); INGREDIENTS: ENRICHED BLEACHED FLOUR (WHEAT FLOUR, MALT BARLEY FLOUR< NIACIN, FERROUS SULFATE, THIAMINE MONONITRATE, RIBOFLAVIN, FOLIC ACID, POTASSIUM BROMATE), WATER, YEAST, SALT, VEGETABLE…
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26V575000·2026-09-07

    Can-Am Recalls Motorcycles Due to Instrument Cluster Freezing Risk

    Bombardier Recreational Products is recalling specific Can-Am motorcycles because the touchscreen instrument cluster may freeze or go blank, hiding critical safety information.

    Product
    CAN-AM — CAN-AM SPYDER RT, SPYDER F3, PULSE, ORIGIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V574000·2026-09-04

    Kibbi Recalls 2026-2027 Renegade RVs Due to Fire Risk

    Kibbi is recalling 2026-2027 Renegade recreational vehicles because a rooftop fan component may overheat and cause a fire.

    Product
    RENEGADE — RENEGADE CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E062000·2026-09-03

    Nova Bus Recalls Casco Engine Coolant Level Sensors

    Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:COOLING SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26739·2026-09-03

    Skip Hop Recalls Elmo Silicone Teethers Due to Choking Hazard

    Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.

    Product
    Baby Sesame Street Elmo Silicone Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26740·2026-09-03

    Truststone Recalls XO Poppy Magnetic Wireless Power Banks Due to Fire Hazards

    Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.

    Product
    XO Poppy Power Trip Magnetic Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26741·2026-09-03

    Clorox Recalls Scented Mistolin and Lestoil Cleaners in Puerto Rico

    Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.

    Product
    Scented Mistolin® Dilutable Cleaners and Lestoil® Heavy Duty Multi-Purpose Cleaners sold in Puerto Rico and the U.S. Virgin Islands.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1271-2026·2026-09-02

    Kettle Cuisine Recalls Marketside Tomato Bisque Soup Kit for Listeria

    Kettle Cuisine is recalling Marketside Tomato Bisque Soup Kits due to a presumptive positive test for Listeria monocytogenes.

    Product
    Marketside Tomato Bisque Soup Kit, Tomato Bisque with Cheese Croutons & White Cheddar Cheese, Ready to Heat, Net Wt. 14 OZ (397g), with UPC 1 94346474004. Must Keep Refrigerated.
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-2988-2026·2026-09-02

    Philips Incisive CT Recalled for Potential Failure to Trigger Clinical Scan

    Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.

    Product
    Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3027-2026·2026-09-02

    Medline Recalls Surgical Convenience Kits Due to Contaminated Components

    Medline Industries is recalling 169 surgical convenience kits nationwide because they contain potentially contaminated components.

    Product
    Medline convenience kits labeled as: 1) LAVH, Medline Kit SKU CDS982273U; 2) GYN ABDOMINAL CDS, Medline Kit SKU CDS982654L; 3) GYN LAP HYSTERECTOMY CDS, Medline Kit SKU CDS982662Q; 4) CMH VAG HYSTERECTOMY PK-LF, Medline Kit SKU DYNJ54382F; 5) A P RESECTION, Medline…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3031-2026·2026-09-02

    Healthmark ProChek-II Medical Tests Recalled for Expired Ingredient

    Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.

    Product
    healthmark ProChek-II, Model Number PT-313, PT-201-12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2998-2026·2026-09-02

    Hollister Recalls Onli Hydrophilic Urethral Catheters Due to Manufacturing Defect

    Hollister is recalling specific lots of Onli hydrophilic urethral intermittent catheters because a manufacturing defect may cause a protrusion that leads to genitourinary trauma or bleeding.

    Product
    Onli 17cm Hydrophilic Urethral Intermittent Catheter, labeled as: 1) 82081 Ch08-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82081; 2) 82101 Ch10-17 Onli Hydrophilic Urethral Intermittent Catheter, SKU/REF 82101; 3) 82121 Ch12-17 Onli Hydrophilic Urethral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1277-2026·2026-09-02

    Byron White Herbal Supplement Recalled for Undeclared Walnut Allergen

    Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.

    Product
    Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
    Category
    Food
    Distribution
    50 states
  • HighFDA (Drugs)·D-0784-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2992-2026·2026-09-02

    Medline Recalls Neonatal Heated Wire Breathing Circuits Due to Thermal Damage

    Medline is recalling 145,525 neonatal and infant heated wire breathing circuits due to potential thermal damage that could cause airway obstruction.

    Product
    Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07); 2) HUDSON RCI, DBM-CIRCUIT,VENT,NEONATAL,21 V, Medline Product Number/SKU HUD78009 (Teleflex Product Number/SKU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3022-2026·2026-09-02

    Medline recalls surgical convenience kits due to potential contamination

    Medline Industries is recalling 94 surgical convenience kits nationwide because they contain a potentially contaminated component.

    Product
    Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4) LAPAROSCOPY, Medline Kit SKU DYNJ903479M.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3034-2026·2026-09-02

    IMRIS ORT300 Operating Room Table Recalled for Mechanical Failure Risk

    IMRIS Imaging Inc is recalling 13 ORT300 operating room tables because a mechanical failure could cause unintended rotational movement, posing a risk of injury to patients.

    Product
    ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
    Category
    Medical Device
    Distribution
    Distributed nationwide