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.

35076–35100 of 50502

  • HighFDA (Food)·F-1826-2016·2016-08-03

    GFS Brownie Cheesecake Recalled for Undeclared Peanut Allergen

    The Father's Table is recalling GFS Brownie Cheesecake because it contains undeclared peanut protein, posing a risk to individuals with peanut allergies.

    Product
    GFS Brownie Cheesecake, 54 oz, 12 cut with papers. Manufactured by The Fathers Table and Distributed by Gordon Food Service.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2274-2016·2016-08-03

    Beckman Coulter Allegra X-5 Rotor Yoke Recalled for Defect

    Beckman Coulter is recalling Allegra X-5 rotor yokes because a defect allows improper rotor seating, which could lead to rotor failure if buckets are loaded in an imbalanced configuration.

    Product
    Allegra X-5 rotor yoke, Catalog No. (Instruments) B30589 and B30590 (Rotor) B30593. Product Labeling: IFU B29071AA. Product Usage: For In Vitro Diagnostic Use. The Allegra X-5 is intended for the separation of components through the use of relative centrifugal force. It is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2295-2016·2016-08-03

    Draeger Babytherm Infant Warmers Recalled for Skin Temperature Mode Risk

    Draeger Medical is recalling 1,599 Babytherm infant warmers due to a risk associated with operating the device in skin temperature mode without a patient connected.

    Product
    Babytherm 8004/8010, Infant Warmer, Class II device, 510 K K971198, Catalog # FR00105 (Babytherm 8010), 2M30404 (Babytherm 8004), non sterile, software controlled. Product Usage: Babytherm 8004/8010 is an open care infant warmer system for warming premature babies, neonates…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16236·2016-08-02

    Starbucks Recalls Stainless Steel Straws Due to Mouth Laceration Risk

    Starbucks is recalling approximately 2.5 million stainless steel straws sold in the U.S. because the rigid design poses a risk of mouth lacerations to young children.

    Product
    Stainless Steel Straws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V574000·2016-08-02

    Hyundai Recalls 2013 Elantra Vehicles for Brake Pedal Stopper Pad Defect

    Hyundai is recalling 64,500 2013 Elantra vehicles because a deteriorating brake pedal stopper pad can prevent the brake light switch from retracting, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16237·2016-08-02

    BYA Sports Recalls Double Hammocks Due to Fall Hazard

    BYA Sports is recalling approximately 760 double hammocks because a weld on the metal ring can fail, causing the hammock to fall and posing a fall hazard to users.

    Product
    Bring Your Adventure (BYA) Sports hammocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V571000·2016-08-02

    Thor Motor Coach Recalls Motorhomes Due to Flammable Shower Curtains

    Thor Motor Coach is recalling specific 2012-2017 motorhomes because the shower curtains may not resist catching fire, increasing injury risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE, ROAD BEAR RENTAL, CITATION, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V569000·2016-08-01

    KME Fire Trucks Recalled for Transmission Power Switching Defect

    KME is recalling 112 fire trucks because a transmission component may fail, preventing operators from switching power output needed for firefighting.

    Product
    KME — KME PREDATOR SS, PREDATOR, PREDATOR PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V567000·2016-08-01

    E-One Recalls 2015-2016 Cyclone II and Typhoon Fire Trucks

    E-One is recalling 2015-2016 Cyclone II and Typhoon fire trucks because a transmission component may fail, preventing the vehicle from pumping water to fight fires.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V563000·2016-07-28

    Mitsubishi Recalls Outlander and Lancer Vehicles for CVT Acceleration Delay

    Mitsubishi is recalling 2015-2016 Outlander Sport, 2016 Outlander, and 2016 Lancer vehicles because a CVT defect may cause acceleration delays, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT, OUTLANDER, LANCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2219-2016·2016-07-27

    WalkMed Infusion Pumps Recalled for Unapproved Software and Specification Changes

    WalkMed Infusion is voluntarily recalling Triton and Triton FP infusion pumps due to unapproved changes to software, specifications, and intended use.

    Product
    The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1727-2016·2016-07-27

    Kellogg Recalls Famous Amos Cookies Due to Undeclared Peanut Allergen

    Kellogg Company is voluntarily recalling Famous Amos Cookies Double Chocolate Chip because of a potential undeclared peanut allergen resulting from a supplier's flour recall.

    Product
    Famous Amos Cookies Double Chocolate Chip, 12 ct., 12.4 oz.
    Category
    Food
    Distribution
    46 states
  • HighFDA (Devices)·Z-2234-2016·2016-07-27

    WalkMed Infusion Recalls IV Sets Due to Potential Particulate Presence

    WalkMed Infusion is voluntarily recalling specific lots of Triton IV administration sets due to the potential presence of particulate matter in or on the devices.

    Product
    T105-000WC IV Set w/2 Y-Sites, BC Vlv & Filter Cap. Packaged in a Tyvek pouch, with 50 pouches per case. Product Usage: Used to administer fluids from a container to a patient through a needle or catheter inserted into a vein.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2242-2016·2016-07-27

    Encore Medical Recalls Modified Linear Standard and Lateral Neck Trials

    Encore Medical is recalling 14 neck trial sets because a retaining ring component can disassemble from the body of the neck.

    Product
    MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1764-2016·2016-07-27

    Parker Products Recalls Choco Praline Graham Blend for Undeclared Peanuts

    Parker Products, Inc. is recalling 725 cases of 3015 Choco Praline Graham Blend due to undeclared peanuts. The product was distributed in Ohio and California.

    Product
    3015 Choco Praline Graham Blend Net Weight: 25 lbs/11.34 kgs
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1723-2016·2016-07-27

    Kellogg Recalls Keebler Frozen Graham Snacks Cinnamon for Undeclared Peanut

    Kellogg Company is voluntarily recalling Keebler Frozen Graham Snacks Cinnamon due to the potential for undeclared peanut allergen resulting from a supplier's flour recall.

    Product
    Keebler Frozen Graham Snacks Cinnamon, 4 ct., 12.7 oz. ; and cups 2.2 oz. 10 ct., and cups 2.2 oz. 8 ct.
    Category
    Food
    Distribution
    46 states
  • HighCPSC·16762·2016-07-27

    Emson Recalls UComfy Neck and Shoulder Heat Wraps Due to Burn Hazard

    Emson is recalling UComfy Neck and Shoulder Heat Wraps because they can overheat and cause burns. Consumers should stop using the product and contact Emson for a free replacement.

    Product
    UComfy Neck and Shoulder Heat Wrap
    Category
    Consumer Product
    Distribution
    Distributed nationwide