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.

40076–40100 of 50506

  • HighNHTSA·14V743000·2014-11-19

    Toyota Recalls Vehicles Due to Seat Heater Wiring Fire Risk

    Toyota is recalling specific models because seat cushion compression may damage heater wiring, creating a fire and injury risk.

    Product
    TOYOTA — TOYOTA HIGHLANDER, CAMRY, PRIUS, SEQUOIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15034·2014-11-19

    Hoppe's Recalls Semi-Auto Gun Bore Cleaner Due to Loose Cap

    Hoppe's is recalling Semi-Auto Gun Bore Cleaner bottles because the child-resistant caps can become loose, posing a risk of chemical ingestion.

    Product
    Hoppe's Semi-Auto Gun Bore Cleaner
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2015·2014-11-19

    DePuy ATTUNE Intuition Distal Femoral Jig Recall for Bushing Defect

    DePuy Orthopaedics is recalling ATTUNE Intuition Distal Femoral Jigs because a pin bushing defect could cause the plastic to fracture or displace during use.

    Product
    ATTUNE Intuition Distal Femoral Jig; sold non-sterile; product is wrapped in bubble wrap and then sealed inside a polyethylene bag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0200-2015·2014-11-19

    Remel Legionella Growth Supplement Recalled for Potential False Negative Results

    Remel Inc is recalling Legionella BCYE Growth Supplement because it may fail to recover Legionella pneumophila, leading to false negative identification.

    Product
    Oxoid Legionella BCYE Growth Supplement SR0110A, packaged in 100 ml vials, 10/pkg. A growth supplement for the isolation of Legionella.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-0498-2015·2014-11-19

    365 Organic Raisin Granola Recalled for Unlabeled Tree Nuts

    Whole Foods Market recalls 365 Organic Raisin Granola because it may contain pecans and coconut not listed on the label.

    Product
    365 Organic Raisin Granola in 17 ounce (482 gram) cardboard cartons; 12 cartons per case. UPC: 099482448738
    Category
    Food
    Distribution
    43 states
  • HighNHTSA·14E079000·2014-11-19

    AFX Recalls FX-76 Motorcycle Helmets for Impact Test Failure

    AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0469-2015·2014-11-19

    Publix Asian Mix Recalled for Undeclared Peanuts

    Publix Bakery Plant is recalling 1,002 cases of Asian Mix clamshells because the product contains peanuts that are not declared on the label.

    Product
    Publix Asian Mix, 14 oz. clamshell containers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0183-2015·2014-11-19

    Siemens Artis zeego C-arm systems recalled for cable routing defect

    Siemens is recalling 164 Artis zeego systems because a cable may be routed incorrectly, potentially causing system failure during procedures.

    Product
    Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0470-2015·2014-11-19

    Pride of Africa Semo Semolina Recalled for Undeclared Wheat

    Raymond-Hadley Corp. is recalling Pride of Africa brand Semo Semolina because label review revealed the product contains undeclared wheat.

    Product
    Pride of Africa brand Semo "Semolina", Net Wt. 5 lb., UPC 016712016918 --- A Product of Raymond-Hadley Corp. Spencer, NY 14883 1-800-252-5220
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0213-2015·2014-11-19

    Masimo SET uSpO2 Pulse Oximetry Cables Recalled for Crossed Wires

    Masimo Corporation is recalling specific SET uSpO2 Pulse Oximetry Cables due to crossed internal wires that may cause the monitoring device to display inverted SpO2 values.

    Product
    Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Cable is an in-line cable that provides continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (Sp02) and pulse rate when installed in a compatible OEM host system. Shipping/Package…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0497-2015·2014-11-19

    Health Wise Recalls Vanilla Pro-Med Shakes Due to Steel Wool Contamination

    Health Wise is recalling 12,196 containers of Vanilla Pro-Med. 100 shakes because steel wool was found in the product.

    Product
    Vanilla Pro-Med. 100, Vanilla Pro, High Protein Instant Shake, Net Weight .0935 oz, Distributed by Our Life Health, Savannah, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0185-2015·2014-11-19

    GE Healthcare Recalls Varicam and VG Hawkeye Nuclear Medicine Devices

    GE Healthcare is recalling 478 nuclear medicine imaging devices because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    GE Healthcare Varicam/VG and VG Hawkeye devices. Models H3000YA, H3000YB, H3000YC, H3000YD, H2508PA, H2508PB, H2508PC, H2508PD. Product Usage: The intended use of the Quasar system is to perform general Nuclear Medicine imaging procedures for detection of radioisotope…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·080-2014·2014-11-19

    K. Heeps Recalls Pork Sausage Due to Undeclared Soy Allergen

    K. Heeps, Inc. is recalling approximately 2,902 pounds of Bratwurst and Bangers sausage products because they contain undeclared soy lecithin, a known allergen.

    Product
    K. Heeps, Inc. — Pennsylvania Firm Recalls Pork Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0197-2015·2014-11-19

    Integra Titan Reverse Shoulder System Cutting Templates Recalled for Manufacturing Error

    Integra LifeSciences Corp. is recalling 12 units of Reverse Shoulder System cutting templates because the threaded handle was welded backwards, resulting in an incorrect cutting angle.

    Product
    Integra Titan Reverse Shoulder System right and left head cutting templates, 142.5 degrees. The Reverse Shoulder System Cutting Template, 142.5 degrees is an accessory for use with the Integra Titan Reverse Shoulder System. It is used to project the osteotomy angle on the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0471-2015·2014-11-19

    Pride of Africa Farina Recalled for Undeclared Wheat

    Raymond-Hadley Corp. is recalling Pride of Africa brand Farina because label review revealed the product contains undeclared wheat.

    Product
    Pride of Africa brand Farina, Net Wt. 5 lb. (2.27 kg), UPC 016712016840 --- A Product of Raymond-Hadley Corp. Spencer, NY 14883 1-800-252-5220
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0502-2015·2014-11-19

    Mondelez Recalls Chiclets Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0189-2015·2014-11-19

    GE Healthcare Recalls Brivo NM615 Nuclear Imaging Systems Due to Loose Fasteners

    GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    Brivo NM615, is an all-purpose, single detector integrated nuclear imaging system. Models H3100TP, H3100TN, H3100TT, H3100TR, H3100TW, H3100WZ, H2401MP, H2401MN, H2401MT, H2401MR, H2401MW, H2401NJ. Product Usage: The Brivo NM 615 is an emission computed tomography system…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0500-2015·2014-11-19

    Mondelez Recalls Chiclets Peppermint Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), Retail UPC 0 12546 10105 9; 2)Chiclets Peppermint Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02501 0, Case UPC 1001254 3)Chiclets Peppermint Gum, (12 pieces), Retail UPC 0 12546 10128 8; 4)Chiclets…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0187-2015·2014-11-19

    GE Healthcare Recalls Discovery NM 630 Nuclear Imaging Systems

    GE Healthcare is recalling 147 Discovery NM 630 nuclear imaging systems to update maintenance procedures and prevent loose fasteners from causing parts to fall on patients.

    Product
    Discovery NM 630, dual detector free-geometry integrated nuclear imaging system. Models H3100RC, H3100RD, H2401LW. Product Usage: The GE Discovery NM 630 system is a medical tool intended for use by appropriately trained healthcare professionals to aid in detecting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2015·2014-11-19

    Roscoe Medical Recalls Transport Rollators Due to Caster Separation Risk

    Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.

    Product
    Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down footrests, ergonomic handles, curved padded backrest and handy wire basket for storage. Item# 30192 Burgundy each/Item# 30194 Blue each.. Transport Rollator is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0499-2015·2014-11-19

    Chiclets Gum Recalled for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Assorted Variety Multipak fruit flavor gum due to undeclared soy lecithin on the label.

    Product
    Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 6-10 piece packages (60 pieces), 6 PAK, Retail UPC 0 12546 10102 8; 2)Chiclets Assorted Variety Multipak - Fruit Flavor Gum, 7-6 PAK packages (420 pieces), Retail UPC 0 12546 0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14T016000·2014-11-19

    Bluestar Trailer Tires Recalled for Sidewall Blister Risk

    China Manufacturers Alliance is recalling specific Bluestar trailer tires that may develop sidewall blisters, potentially causing loss of vehicle control.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V735000·2014-11-18

    Isuzu Recalls 2012-2014 Reach Chassis Due to Brake Light Switch Defect

    Isuzu is recalling 3,564 model year 2012-2014 Reach chassis because the brake light switch may bend or corrode, potentially failing to activate brake lights and increasing crash risk.

    Product
    ISUZU — ISUZU REACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15028·2014-11-18

    Black Diamond Recalls Whippet Ski Poles Due to Pick Breakage Risk

    Black Diamond Inc. is recalling Whippet and Carbon Whippet ski poles because the stainless steel pick can break, posing a risk of injury to users on slopes.

    Product
    Ski poles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V736000·2014-11-18

    Ford Recalls Fusion Models Due to Key Removal Safety Defect

    Ford is recalling 2014-2015 Fusion, Fusion Hybrid, and Fusion Energi vehicles because the key may be removed while the transmission is not in Park, increasing the risk of rollaway.

    Product
    FORD — FORD FUSION, FUSION HYBRID, FUSION ENERGI
    Category
    Vehicle
    Distribution
    Distributed nationwide