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.

41801–41825 of 50511

  • HighCPSC·14114·2014-02-25

    Genie Recalls Garage Door Openers Due to Fire Hazard

    Genie is recalling specific screw drive garage door openers because the control board can overheat, posing a fire hazard. No injuries have been reported.

    Product
    Garage door openers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14113·2014-02-25

    Rollerblade USA Recalls Tempest Inline Skates Due to Fall Hazard

    Rollerblade USA is recalling about 11,800 pairs of Tempest inline skates because misaligned mounting holes can cause the boot to separate from the frame, posing a fall hazard.

    Product
    Rollerblade® Tempest Inline Skates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V088000·2014-02-21

    Mack LEU Trucks Recalled for Exhaust Pipe Disconnection Risk

    Mack is recalling 2010-2015 LEU trucks with Cummins ISL engines because the exhaust pipe may disconnect, potentially exposing operators to carbon monoxide.

    Product
    MACK — MACK LEU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14110·2014-02-20

    U.S. Polo Assn. Recalls Girl's Jackets Due to Strangulation Hazard

    U.S. Polo Assn. is recalling girl's jackets because a neck band poses a strangulation hazard to young children. No injuries have been reported.

    Product
    U.S. Polo Assn. girl's jackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14109·2014-02-20

    Infantino Recalls Teething Toys Due to Choking Hazard

    Infantino is recalling Go Gaga Squeeze & Teethe Coco the Monkey teething toys because the tail poses a choking hazard to young children.

    Product
    Go Gaga Squeeze & Teethe Coco the Monkey
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V076000·2014-02-20

    Intercontinental Truck Cube Van Door Lock Recall for Jamming Risk

    Intercontinental Truck Body is recalling 2010-2013 Cube Vans because a door lock defect may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    INTERCONTINENTAL TRUCK — INTERCONTINENTAL TRUCK CUBE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14108·2014-02-20

    Sterling Rope Recalls Sewn Cords Due to Fall Hazard

    Sterling Rope Company is recalling specific sewn cord products because they may break at lower weights than published, posing a fall hazard.

    Product
    Sewn cord edge restraints, sewn eyes and sewn loops.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14107·2014-02-19

    Lucent Ace Recalls LED Flashlights Due to Burn Hazard

    Lucent Ace Manufacturing is recalling about 3,000 LED flashlights sold at Academy Sports + Outdoors because the battery can short and cause the canister to rupture, posing a burn hazard.

    Product
    LED flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0969-2014·2014-02-19

    Boston Scientific Recalls Coyote Balloon Dilation Catheters Due to Deflation Issues

    Boston Scientific is recalling specific lots of Coyote balloon dilation catheters because the balloons may not deflate as expected during procedures.

    Product
    Boston Scientific, 2.5mm Coyote" OVER-THE-WIRE PTA Balloon Dilation Catheter, UPN# H74939186251210, Catalog # 39186-25121.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-1484-2014·2014-02-19

    Araya Chocolate Gift Boxes Recalled for Undeclared Allergens

    Araya, Inc. is recalling specific chocolate gift boxes nationwide because they may contain undeclared allergens. Consumers should stop using these products.

    Product
    Chocolate Gift Boxes: SC 6 Oreos, SC Small 12 Chocolate, SC Small 6 chocolate Araya Artisan Chocolate: 1545 W Grand Parkway S, Katy, TX, 77494 Tlf (281) 395-1050 [email protected]
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0971-2014·2014-02-19

    Boston Scientific Recalls Coyote PTA Balloon Dilatation Catheters

    Boston Scientific is recalling Coyote PTA Balloon Dilatation Catheters because the balloons may not deflate as expected during procedures.

    Product
    Boston Scientific, Coyote" MONORAIL" PTA Balloon Dilatation Catheter, UPN # H74939185201510, Catalogue # 39185-20151.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0967-2014·2014-02-19

    Brainlab VectorVision Spine Instrument Star Unit ML Recall

    Brainlab is recalling 25 VectorVision Spine Instrument Star Unit ML devices because pins may be made of incorrect material, posing a risk of corrosion and particle release during surgery.

    Product
    BrainLAB's VectorVision spine is intended for use as an intraoperative image-guided localization system for minimally invasive surgery. It links a freehand probe, tracked by a passive marker sensor system to virtual computer image space on a patient's preoperative image data…
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-0976-2014·2014-02-19

    McKesson Recalls Horizon Medical Imaging PACS Software Due to Archive Errors

    McKesson Information Solutions LLC is recalling 618 units of Horizon Medical Imaging PACS software because images may be archived to incorrect locations, causing display failures.

    Product
    Horizon Medical Imaging, Picture Archive Communication System (PACS).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0947-2014·2014-02-19

    Ecolab Recalls Microtek Medical Bur Hole Latex Probe Covers

    Ecolab Inc is recalling specific lots of Microtek Medical Bur Hole Latex Probe Covers because they did not undergo proper endotoxin testing.

    Product
    MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER WITH GEL, featuring IsoSilk(R), 13cm x 249 cm, REF 3688UK, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1483-2014·2014-02-19

    Araya Chocolate-Covered Fruits Recalled for Undeclared Allergens

    Araya, Inc. is recalling chocolate-covered dry fruits due to potential undeclared allergens. The products were distributed nationwide.

    Product
    Dry fruits covered in chocolate in the following flavors: orange peel, mango cayenne, pear Araya Artisan Chocolate: 1545 W Grand Parkway S, Katy, TX, 77494 Tlf (281) 395-1050 [email protected]
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2014·2014-02-19

    Custom Medical Specialties Recalls Ultrasound Probe Covers for Missing Endotoxin Testing

    Custom Medical Specialties is recalling 2,610 sterile ultrasound probe covers because they were not tested for endotoxins to the required level.

    Product
    5 x 93 US Probe Cover CMS-6049, Sterile, Single Patient Use. Custom Medical Specialties, Inc., Pine Level, NC, Federal (USA) law restricts this device to the sale by or on the order of a physician. Probe cover
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-1475-2014·2014-02-19

    Farm To Market Bread Co. Sourdough Recalled for Undeclared Wheat

    Farm To Market Bread Co. is recalling San Francisco Sourdough bread because the label fails to list wheat flour, an undeclared allergen.

    Product
    Farm To Market Bread Co. San Francisco Sourdough, net weight 1 lb., unbleached enriched flour, water, sea salt, vitamin C. Farm to Market Bread Co., Kansas City, MO.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0979-2014·2014-02-19

    Philips Gemini TF Big Bore PET/CT Systems Recalled for Mechanical Binding

    Philips is recalling 47 Gemini TF Big Bore PET/CT systems because the patient table can mechanically bind, causing an automatic emergency stop and incomplete scans.

    Product
    GEMINI TF Big Bore PET/CT, Computer Tomography System, Philips Healthcare System, Cleveland, OH
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Food)·F-1481-2014·2014-02-19

    Araya Gourmet Chocolate Bars Recalled for Undeclared Allergens

    Araya, Inc. is recalling specific gourmet chocolate bars nationwide because they may contain undeclared allergens. Consumers should check their packages for the listed UPC codes.

    Product
    Gourmet Bar in the following flavors: bacon, cayenne pepper, crispy orange, curry, mendiant dark, mendiant light Araya Artisan Chocolate: 1545 W Grand Parkway S, Katy, TX, 77494 Tlf (281) 395-1050 [email protected]
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1480-2014·2014-02-19

    Windsor Frozen Foods Recalls Gorgonzola Gems Jalapeno Peppers Due to Listeria Risk

    Windsor Frozen Foods is recalling Gorgonzola Gems Jalapeno Peppers because the product has the potential to be contaminated with Listeria monocytogenes.

    Product
    Gorgonzola Gems Jalapeno Peppers With Gorgonzola and Cream Cheese Blend 8 oz. (227 g) packages, 6/pack
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0948-2014·2014-02-19

    Ecolab Recalls Vital Care Ultrasound Probe Covers Due to Testing Deficiencies

    Ecolab Inc is recalling specific lots of Vital Care ultrasound probe covers because they did not undergo endotoxin testing to the proper levels.

    Product
    Vital CARE(TM) REPS INC. ULTRASOUND PROBE COVER, BUR HOLE COVER, 5 x 96, REF VPC0699, STERILE EO, QTY 20, Manufactured for Vital Care Reps, Inc., Tinley Park, Illinois
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0946-2014·2014-02-19

    Ecolab Recalls Microtek Medical Bur Hole Latex Probe Covers

    Ecolab Inc is recalling specific lots of Microtek Medical Bur Hole Latex Probe Covers because they did not undergo endotoxin testing to the proper levels.

    Product
    MICROTEK(TM) MEDICAL BUR HOLE LATEX PROBE COVER W/ GEL, featuring IsoSilk(R), 5" x 98", (13cm x 249 cm), REF 3688, STERILE EO, QTY 20, Microtek Medical, Inc., Columbus, MS 39702
    Category
    Medical Device
    Distribution
    Distributed nationwide