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.

32251–32275 of 50502

  • HighFDA (Drugs)·D-0757-2017·2017-05-24

    Key Pharmacy Recalls PGE1/Procaine Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of PGE1/Procaine injection because the firm cannot ensure the sterile compounded drugs are free from contamination.

    Product
    PGE1/PROCAINE 5ML MDV 40MCG/ML/0.1% INJ, Injection, 40mcg/mL, 0.1%, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2227-2017·2017-05-24

    Kemps Recalls Frozen Yogurt and Ice Cream Due to Plastic Contamination

    Kemps, LLC is recalling select pints of Sweet Me Creamery Ice Cream and YO2 Frozen Yogurt because they may contain pieces of plastic.

    Product
    Kemps YO2 Frozen Yogurt Raspberry Cheesecake, One Pint, UPC 41483-04127
    Category
    Food
    Distribution
    20 states
  • HighFDA (Drugs)·D-0772-2017·2017-05-24

    Key Pharmacy Recalls Procaine HCL Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Procaine HCL 1% injections because the firm cannot ensure the products are sterile.

    Product
    PROCAINE HCL *5ML* SDV SULFITE FREE 1% INJ, Injection, 1%, RXxonly, 5mL Glass/Single Dose vials, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0722-2017·2017-05-24

    Key Pharmacy Recalls Hydroxo-B12 Injections Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of Hydroxo-B12 injections because the firm cannot assure the sterility of the products.

    Product
    HYDROXO-B12 1ML SDV 10MG/ML INJ, Injection, 10mg/mL, Rx only, 1 mL glass/ Single Dose vial, Prepared by Key Compounding Pharmacy HYDROXO-B12 2ML SDV 10MG/ML INJ, Injection, 10mg/mL, RX only, 2 mL glass/ Single Dose vial.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V339000·2017-05-24

    Keystone Springdale RVs Recalled for Incorrect Weight Rating Labels

    Keystone is recalling 2012-2018 Springdale 303BH RVs because Federal Identification Tags overstate axle weight capacity, potentially leading to vehicle overload.

    Product
    KEYSTONE — KEYSTONE SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2092-2017·2017-05-24

    Vortran Automatic Resuscitator Recalled Due to Reverse-Threaded Oxygen Connector

    Vortran is recalling 14 cases of VARPlus Automatic Resuscitators because the oxygen tubing connector was assembled in reverse, preventing it from being screwed on.

    Product
    VORTRAN Automatic Resuscitator, VARPlus with Extension Kit; Model PCE-5012; Qty: 10 each. Anesthesiology: This device is to be used by properly trained personnel to deliver emergency, short term, constant flow, pressure cycled ventilatory support.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2110-2017·2017-05-24

    Molnlycke Recalls Brennen Skin Graft Mesher Due to Sterilization Failure

    Molnlycke Health Care is recalling 956 units of the Brennen Skin Graft Mesher because of a sterilization validation failure. The instruments were distributed domestically and internationally.

    Product
    Brennen Skin Graft Mesher. Surgical instrument designed to expand skin grafts'
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2105-2017·2017-05-24

    Medline Recalls 10 mm Distraction Pins Due to Sterile Seal Concerns

    Medline Industries is recalling 10 mm Distraction Pins because the sterile packaging seal may be compromised, potentially causing the device to lose sterility.

    Product
    10 mm Distraction Pin, Aggressive Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2094-2017·2017-05-24

    Luminex ARIES System Recalled for Barcode Scanner Data Error

    Luminex Corporation is recalling 15 ARIES Systems because a barcode scanner accessory may incorrectly populate patient sample IDs with previously scanned data.

    Product
    ARIES System and ARIES M1 System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2218-2017·2017-05-24

    Whole Foods Recalls Holiday Cookies Due to Undeclared Wheat

    Whole Foods Market is recalling 216 decorated holiday cookies sold in the Bay Area because they contain undeclared wheat.

    Product
    Decorated (iced) holiday cookies sold in the shape of eggs. These cookies were sold in the self service cookie displays. Individual cookies are 1.3 oz.. each. Cookie labels identify the cookies as: Sugared Purple Egg Cookies: Sugar Pink Bunny Cookie; Sugared Yellow Chick…
    Category
    Food
    Distribution
    0 states
  • HighCPSC·17164·2017-05-23

    Pier 1 Imports Recalls Temani Wicker Furniture for Lead Paint Violation

    Pier 1 Imports is recalling Temani wicker chairs, settees, and ottomans because the paint may contain excessive lead, violating federal standards.

    Product
    Temani ivory wicker chair, settee and ottoman
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17166·2017-05-23

    Hobby Lobby Recalls Easter and July 4th Light-Up Spinner Toys

    Hobby Lobby is recalling Easter and July 4th-themed light-up spinner toys because the battery cover can detach, exposing coin cell batteries that pose choking and ingestion hazards to young children.

    Product
    Easter and July 4th-themed Light-Up Spinner Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V334000·2017-05-23

    REV Road Rescue Emergency Vehicles Recalled for Cot Securing Bolt Defect

    REV is recalling 24 Road Rescue emergency vehicles because short bolts may fail to secure the cot during a crash, potentially injuring occupants.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE IX, TYPE I, TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V335000·2017-05-23

    Keystone Recalls 2017-2018 Dutchmen Voltage Trailers Due to Fuel Line Defect

    Keystone RV Company is recalling 2017-2018 Dutchmen Voltage trailers with Onan 5.5 generators because an incorrectly clamped fuel line may disconnect, causing a fuel leak and fire risk.

    Product
    DUTCHMEN — DUTCHMEN VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17162·2017-05-23

    Dynacraft Recalls Ride-On Toys Due to Sticking Pedal Hazard

    Dynacraft is recalling about 20,000 Surge and Tonka battery-operated ride-on toys because the acceleration pedal can stick, posing fall and crash hazards.

    Product
    Surge and Tonka battery operated ride-on toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17T010000·2017-05-23

    Kenda Kenetica Tires Recalled for Steel Belt Void Risk

    American Kenda Rubber Industrial is recalling specific Kenetica tires due to a void in the steel belt that may cause tread separation or sudden air loss.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V333000·2017-05-22

    Harley-Davidson Recalls 2017 Motorcycles Due to Oil Cooler Line Clamp Defect

    Harley-Davidson is recalling 45,589 2017 motorcycles because an improperly installed clamp may cause the engine oil cooler line to detach, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCU, FLTRX, FLHTP, FLHRXS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-051617-exp·2017-05-20

    Imported Veal Products Recalled Over Possible E. coli O103 Contamination

    USDA FSIS issued a Public Health Alert for approximately 1,631 pounds of raw veal products imported from the Netherlands due to possible contamination with Non-O157 Shiga toxin-producing E. coli O103. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert For Imported Veal Products Due To Possible Non-O157 Shiga toxin producing E. coli (STEC) O103 Contamination
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·17V326000·2017-05-18

    Ferrara Recalls Fire Apparatus Due to Guardrail Defect

    Ferrara is recalling 2000-2016 Fire Apparatus 100' Platform vehicles because a movable ladder access guardrail may bend or break under heavy loads, increasing injury risk.

    Product
    FERRARA — FERRARA APPARATUS 100' PLATFORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17156·2017-05-18

    Pier 1 Imports Recalls Chalk Note Mugs Due to Burn Hazard

    Pier 1 Imports is recalling Chalk Note Mugs because they can crack when filled with hot liquid, posing a burn hazard to users.

    Product
    Chalk Note Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide