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.

32201–32225 of 50502

  • HighFDA (Devices)·Z-2133-2017·2017-05-31

    Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Flat Drains

    Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.

    Product
    Jackson-Pratt Hemaduct Silicone Flat Drain, 10mm, Full Ducts W/15FR Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2017·2017-05-31

    Merge Cardio software recalled for incorrect fetal measurement data retrieval

    Merge Healthcare is recalling Merge Cardio software versions 10.0 through 10.1.2 because the software may display incorrect fetal measurements by pulling data from prior pregnancies.

    Product
    Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to be used to acquire, store, print, transfer, and archive clinical information.
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-2141-2017·2017-05-31

    Cardinal Health Recalls Jackson-Pratt Silicone Flat Drains Due to Sterility Concerns

    Cardinal Health is recalling specific lots of Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially increasing the risk of infection.

    Product
    Jackson-Pratt Silicone Flat Drain, 7mm, 3/4 Ducts. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2160-2017·2017-05-31

    Stryker Recalls Hoffmann LRF Safety Clips Due to Loosening Risk

    Stryker is recalling Hoffmann LRF Safety Clips because they may loosen from the Quick Release mechanism on Transport Struts.

    Product
    Hoffmann LRF Safety Clip (Bone Transport Strut), 14 x 12 x 5 mm, REF 4933-0-401, NDC (01)07613327131475(10)V07241 Product Usage: Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, and bone and soft tissue reconstruction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2148-2017·2017-05-31

    Cardinal Health Recalls Jackson-Pratt Silicone Round Drains Due to Sterility Concerns

    Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.

    Product
    Jackson-Pratt Silicone Round Drain, 19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V347000·2017-05-30

    KZRV Venom Travel Trailer Recall for Fire Risk

    KZRV is recalling 2016-2018 Venom fifth-wheel travel trailers with outside kitchens because a missing copper pipe may cause the gas line to melt and start a fire.

    Product
    KZRV — KZRV VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V350000·2017-05-30

    Jayco Eagle Travel Trailer Recalled for Incorrect Weight Rating Label

    Jayco is recalling 2018 Eagle TT 330RSTS trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to overloading and loss of control.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V344000·2017-05-26

    Gulf Stream Travel Trailer Recall for Incorrect Tire Identification Label

    Gulf Stream is recalling 2015-2018 Vista and Vintage Cruiser travel trailers because the tire label lists incorrect tire specifications, which could lead to installing the wrong replacement tires.

    Product
    GULF STREAM — GULF STREAM VISTA CRUISER, VINTAGE CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17168·2017-05-26

    CPSC Recalls Kobalt and Greenworks Cordless Lawn Mowers Due to Fire Hazard

    CPSC is recalling about 28,000 Kobalt and Greenworks cordless electric lawn mowers because the circuit board can short circuit and catch fire. No injuries have been reported.

    Product
    Cordless electric lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V346000·2017-05-26

    Forest River Recalls 2016-2017 Vibe Trailers for Incorrect Tire Placard

    Forest River is recalling 2016-2017 Vibe recreational trailers because the Federal Placard lists incorrect tire size and pressure information, which could lead to improper tire maintenance.

    Product
    FOREST RIVER — FOREST RIVER VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V341000·2017-05-25

    Jaguar Recalls 2018 F-TYPE for Turn Signal Reminder Defect

    Jaguar is recalling 2018 F-TYPE vehicles with Highline headlamps because the turn signal reminder may not flash or chime faster if a signal fails, increasing crash risk.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17167·2017-05-25

    Extech Recalls Digital Clamp Meters Due to Electrocution Hazard

    Extech is recalling specific digital clamp meters because they may display incorrect voltage readings, posing an electrocution risk to operators.

    Product
    Digital clamp meters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2093-2017·2017-05-24

    Spacelabs Arkon Anesthesia Delivery System Canister Carrier Recall

    Del Mar Reynolds Medical is recalling 62 Spacelabs Arkon Anesthesia Delivery System components because the canister carrier can break, causing a breathing circuit leak and potential patient hypoventilation.

    Product
    Spacelabs Healthcare Arkon Anesthesia Delivery System is intended for use in the hospital environment and operating room. Absorber Adapter Assembly Service Kit, part number: 050-9045-00. Absorber Adapter Assembly, part number: 650-1648-01. Arkon Absorber Canister Carrier…
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-2155-2017·2017-05-24

    Raley's Muesli Almond Crunch Cereal Recalled for Missing Coconut Allergen Labeling

    Raley's is recalling Muesli Almond Crunch Cereal because an internal review found coconut was not listed in the allergen declaration. The product was distributed in California and Nevada.

    Product
    RALEY'S MUESLI ALMOND CRUNCH MUESLI CEREAL; 12 oz. box - foil bag inside paper box. UPC: 46567-02263; Product Distributed by Raley's, West Sacramento, CA; Product of Switzerland
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2231-2017·2017-05-24

    Kemps Sweet Me Creamery Ice Cream Recalled for Plastic Contamination

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

    Product
    Kemps Sweet Me Creamery Creamy Dark Chocolate Mint, One Pint, UPC 41483-04143
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·F-2237-2017·2017-05-24

    Full Tilt Ice Cream Recalls Vegan Fudge Brownie Swirl for Undeclared Wheat

    Full Tilt Ice Cream is recalling 2,862 pints of Fudge Brownie Swirl Vegan ice cream because the product contains flour but does not declare wheat as an allergen.

    Product
    Label reads in part "***Full Tilt Ice Cream Fudge Brownie Swirl Vegan***one pint***Ingredients: Coconut Milk (coconut milk, water, citric acid), organic evaporated cane juice, bownie bits (flour, sugar, cocoa powder, non-aluminum baking powder, salt, vanilla extract, coconut…
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V337000·2017-05-24

    MCI Recalls 2011-2012 Coaches Due to Exhaust Pipe Fire Risk

    Motor Coach Industries is recalling 2011-2012 MCI D4000, D4005, D4500, and D4505 coaches because an incorrectly installed exhaust bellow pipe may bend and fail, increasing the risk of fire.

    Product
    MCI — MCI D4500, D4000, D4505, D4005
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2077-2017·2017-05-24

    Ortho-Clinical enGen Laboratory Automation Systems Recalled for Software Anomaly

    Ortho-Clinical Diagnostics is recalling enGen Laboratory Automation Systems due to a software anomaly that may cause sample ID misassociation, potentially leading to misdiagnosis.

    Product
    enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication Interface, IVD
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Food)·F-2154-2017·2017-05-24

    Raley's Muesli Red Berry Crunch Cereal Recalled for Missing Coconut Allergen

    Raley's is recalling Muesli Red Berry Crunch Cereal because an internal review found coconut was not listed in the allergen declaration.

    Product
    RALEY'S MUESLI RED BERRY CRUNCH CEREAL; 12 oz. box - foil bag inside paper box. UPC: 46567-02264;product Distributed by Raley's, West Sacramento, CA;Product of Switzerland
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0738-2017·2017-05-24

    Key Pharmacy Recalls Sterile Compounded Drug Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling specific lots of TRI MIX 10/30/1 injection due to a lack of assurance of sterility.

    Product
    TRI MIX 10/30/1 5ML MDV MCG/MG/MG/ML INJ, Injection, 10mcg/30mg/1mg/mL, Rx only, 5 mL Glass/ Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2091-2017·2017-05-24

    Vortran VARPlus Automatic Resuscitator Recalled Due to Connector Assembly Error

    Vortran is recalling 35 cases of VARPlus Automatic Resuscitators because a connector was assembled in the reverse direction, preventing it from screwing onto the oxygen tubing.

    Product
    VORTRAN Automatic Resuscitator, VARPlus; Model PTE-5002; 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 (Food)·F-2219-2017·2017-05-24

    Moondance Gluten-Free Chocolate Chip Cookie Bars Recalled for Undeclared Milk

    Moondance Heavenly Desserts is recalling gluten-free Chocolate Chip Cookie Bars because they contain undeclared milk. The product was distributed to nine states.

    Product
    Moondance desserts gluten free Chocolate Chip Cookie Bar 12 oz (340g) UPC 36211 68096 9
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-2233-2017·2017-05-24

    Kemps Sweet Me Creamery Ice Cream Recalled for Plastic Contamination

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

    Product
    Kemps Sweet Me Creamery Strawberry Rhubarb Cobbler, One Pint, UPC 41483-04145
    Category
    Food
    Distribution
    20 states