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.

31226–31250 of 50502

  • HighFDA (Food)·F-2956-2017·2017-08-09

    Sami's Bakery Walnut Chocolate Chip Cookies Recalled for Undeclared Milk

    Sami's Pita Bakery, Inc. is recalling Walnut Chocolate Chip Cookies because they contain undeclared milk, a major food allergen.

    Product
    SAMI'S BAKERY, Walnut Chocolate Chip Cookies, Net Wt. 7oz. (196g), Packed by: Sami's Pita Bakery Inc., Tampa, FL.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2760-2017·2017-08-09

    Olympus VANTA Analytical X-Ray System Recalled for Proximity Shutdown Failure

    Olympus is recalling 146 VANTA Analytical X-Ray Systems because they may fail to stop testing when no sample is present.

    Product
    Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System, X-Ray Fluorescence
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2786-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach

    LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a potential sterile barrier breach.

    Product
    SORIN GROUP, SMART PERFUSION PACK, INSPIRE 6FS, REF 044008204, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2863-2017·2017-08-09

    Spectranetics Turbo-Elite Laser Atherectomy Catheters Recalled for Marker Band Risk

    Spectranetics is recalling Turbo-Elite Laser Atherectomy Catheters because a marker band may become loose or disengaged when the device is used off-label.

    Product
    Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in the treatment, including atherectomy, of infrainguinal stenosis and occlusions
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Food)·F-2954-2017·2017-08-09

    Sami's Bakery Peanut Butter Cookies Recalled for Undeclared Milk Allergen

    Sami's Pita Bakery, Inc. is recalling Peanut Butter Cookies because they contain undeclared milk, a major food allergen.

    Product
    SAMI'S BAKERY, Peanut Butter Cookies, Net Wt. 7oz. (196g), Packed by: Sami's Pita Bakery Inc., Tampa, FL.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2783-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach

    LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.

    Product
    SORIN GROUP, SMART PERFUSION PACK, LONG PACK, REF 088512600, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2790-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach

    LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.

    Product
    SORIN GROUP, SMART PERFUSION PACK, SMART 3/16" PEDS PACK, REF 627263601, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2865-2017·2017-08-09

    SoftLab Software Recalled for Incorrect Lab Result Display

    Soft Computer Consultants is recalling SoftLab Software versions 4.5.4.3 through 4.5.5.20 because it may display lab results based on incorrect LOINC codes.

    Product
    SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by knowledgeable, trained,
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2794-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach

    LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.

    Product
    SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8S, REF 044036101, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2789-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterility Breach

    LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.

    Product
    SORIN GROUP, SMART PERFUSION PACK, PUMP AND TABLE PACK, REF 627374101, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2785-2017·2017-08-09

    LivaNova Perfusion Tube Sets Recalled for Potential Sterile Barrier Breach

    LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes that compromise sterility.

    Product
    SORIN GROUP, SMART PERFUSION PACK, SMA PRIMO2X OPTI PACK, REF 088512900, STERILE EO, Rx Only, 1 EA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17E045000·2017-08-08

    Hickory Springs Recalls CE White Convertible School Bus Seats

    Hickory Springs is recalling CE White Convertible School Bus Seats due to inadequate padding on D-ring mounting studs, which may increase injury risk in rear-end collisions.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17203·2017-08-08

    Polaris Recalls Scrambler All-Terrain Vehicles Due to Throttle Switch Failure

    Polaris is recalling 2,800 Scrambler XP 1000 ATVs because the throttle release switch can fail, posing a crash hazard. Consumers should stop using the vehicles and contact Polaris for a free repair.

    Product
    Polaris Scrambler all-terrain vehicle (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17201·2017-08-08

    NVIDIA Recalls European Plug Heads for Power Adaptors Due to Shock Hazard

    NVIDIA is recalling European plug heads for SHIELD power adaptors because they can break and expose metal prongs, posing an electric shock hazard.

    Product
    European plug heads for NVIDIA SHIELD™ power adaptors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E044000·2017-08-07

    K&N Recalls Powersports Oil Filters for Leak Risk

    K&N Engineering is recalling specific Powersports Oil Filters that may leak oil onto the rear tire or brake, increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17761·2017-08-07

    Firewood Recalls Vaporizers Due to Fire Hazard

    Firewood is recalling about 400 Firewood 4 vaporizers because an electrical short can cause the battery to catch fire. No injuries have been reported.

    Product
    Vaporizers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·088-2017·2017-08-05

    Hahn Brothers Recalls Ready-to-Eat Ham for Undeclared Malted Barley Allergen

    Hahn Brothers is recalling 115,773 pounds of ready-to-eat ham products because they contain malted barley, an allergen not listed on the label.

    Product
    Hahn Brothers, Inc. Recalls Ready-To-Eat Ham Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V487000·2017-08-03

    GM Recalls 2017 Silverado and Sierra Trucks for Missing Child Seat Instructions

    General Motors is recalling 2017 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because the owner's manual may lack instructions for child restraint anchorage systems.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2903-2017·2017-08-02

    ICYBAY Raw Breaded Cod Nuggets Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling ICYBAY Raw Breaded Natural Shaped Cod Nuggets due to an undeclared milk allergen.

    Product
    ICYBAY Raw Breaded Natural Shaped Cod Nuggets 1 OZ - NET Wt. 10 LBS. (4.54Kg)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2906-2017·2017-08-02

    Ocean's Best Raw Breaded Fish Squares Recalled for Undeclared Milk Allergen

    Channel Fish Processing Co. Inc. is recalling Ocean's Best Raw Breaded Fish Squares because the product contains undeclared milk, a major food allergen.

    Product
    Ocean's Best Raw Breaded Fish Squares - 4 OZ COD. - Net Wt. 10 lb. (4.54KG)
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-2877-2017·2017-08-02

    Nelson's Dutch Farms Ice Cream Recalled for Undeclared Soy Allergen

    Nelson's Creamery is recalling Cinnamon Carmel Swirl ice cream because the labels failed to declare soy as an ingredient.

    Product
    Nelson's Dutch Farms; Cinnamon Carmel Swirl; Half Gallon; Nelson's Ice Cream, Inc., Royersford, PA 19468
    Category
    Food
    Distribution
    3 states