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.

36601–36625 of 50504

  • HighCPSC·16111·2016-03-01

    United Pet Group Recalls Top Fin Aquarium Power Filters for Shock Hazard

    United Pet Group is recalling Top Fin power filters for aquariums because a conductor can expose consumers to electric shock. No injuries have been reported.

    Product
    Top Fin™ Power Filters for Aquariums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E016000·2016-03-01

    Carquest DOT5 Silicone Brake Fluid Recalled for Labeling Defects

    American Grease Stick Company is recalling Carquest DOT5 Silicone Brake Fluid bottles manufactured between October 2013 and September 2015 due to missing or unclear labeling required by federal safety standards.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16110·2016-03-01

    Ambient Weather Radios Recalled Due to Fire Hazard

    Ambient Weather is recalling about 57,000 radios that can overheat when plugged into AC power, posing a fire hazard.

    Product
    Ambient Weather radios
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V117000·2016-02-29

    Hyundai Recalls Equus and Genesis Vehicles for Wiper Motor Defect

    Hyundai is recalling 2011-2013 Equus and 2012 Genesis vehicles because a degrading wiper motor seal can cause corrosion and loss of wiper function, increasing crash risk in bad weather.

    Product
    HYUNDAI — HYUNDAI EQUUS, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V118000·2016-02-29

    Terex Recalls 2008-2015 Aerial Devices Due to Cylinder Contact Risk

    Terex is recalling 2008-2015 aerial devices because cylinder components may contact structural parts, potentially causing platform tilting and occupant falls.

    Product
    TEREX — TEREX AERIAL DEVICES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V115000·2016-02-26

    Open Range Recalls 2012-2014 Trailers Due to Incorrect Weight Labels

    Open Range is recalling 2012-2014 Mesa Ridge, Roamer, and Light trailers because incorrect Gross Vehicle Weight Rating labels may lead to overloading.

    Product
    OPEN RANGE — OPEN RANGE LIGHT, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V110000·2016-02-25

    Ford Recalls 2016 F-150 Trucks Due to Air Bag Sensor Defect

    Ford is recalling 2016 F-150 trucks with Multi-Contour Seats because the passenger air bag sensor may misclassify adults as children, preventing air bag deployment.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V111000·2016-02-25

    Ford Recalls 2015-2016 Transit Vehicles for Rear Seat Belt Defect

    Ford is recalling 2015-2016 Transit vans because rear seat belt buckles may fail to latch if damaged by heavy objects, increasing crash injury risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0818-2016·2016-02-24

    Smith & Nephew Recalls High Flow Irrigation Extender for Separation Risk

    Smith & Nephew is recalling 203 High Flow Irrigation Extenders because the device body may separate during surgery, potentially obstructing visualization and causing fluid leakage.

    Product
    High Flow Irrigation Extender; Part Number 72201021. Arthroscopic accessories are indicated for use in access of the joint capsule.
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Food)·F-0586-2016·2016-02-24

    Kwik Trip Bakery Recalls Plain Long Johns Due to Plastic Contamination

    Kwik Trip Bakery is recalling Plain Long Johns that may contain plastic pieces from contaminated ice nuggets used as an ingredient.

    Product
    Plain Long Johns 9999954013, 540138 each, product shipped frozen (28 per bulk tote).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0714-2016·2016-02-24

    Abbott's Compounding Pharmacy Recalls Sterile Compounded Products Due to Sterility Concerns

    Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, after FDA inspection found concerns regarding lack of sterility assurance.

    Product
    papaverine phentolamine prostaglandin; 9/1 mg/10 mcg/mL, 10 mL, unit size, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0691-2016·2016-02-24

    Abbott's Compounding Pharmacy Recalls Sterile Compounded Products Due to Sterility Concerns

    Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine, after FDA inspection found concerns regarding lack of sterility assurance.

    Product
    papaverine phentolamine, 35 mg/2.5 mg/mL; 5 mL unit size; refrigerate,This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0687-2016·2016-02-24

    Abbott's Compounding Pharmacy Recalls Methylcobalamine Due to Sterility Concerns

    Abbott's Compounding Pharmacy is recalling all unexpired lots of methylcobalamine 4 mg/mL in California due to FDA findings of lack of sterility assurance.

    Product
    methylcobalamine 4 mg/mL, 5 mL and 30 mL unit sizes, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
    Category
    Drug
    Distribution
    1 state
  • HighCPSC·16109·2016-02-24

    England's Stove Works Recalls Smartstove Pellet Stoves for Laceration Hazard

    England's Stove Works is recalling about 2,300 Smartstove freestanding pellet stoves because ash accumulation can cause the door glass to break, posing a laceration hazard.

    Product
    Smartstove freestanding pellet stoves
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0807-2016·2016-02-24

    Bio-Rad EVOLIS Microplate System Recalled for Plate Transport Hazard

    Bio-Rad is recalling 278 EVOLIS Microplate Systems because a low fluid alarm could cause the plate transport to continue running, pushing plates off the transporter.

    Product
    EVOLIS Microplate System, Catalog # 89601. Part number 89788 for the EVOLIS Operator's Manual. in vitro diagnostic Product Usage: EVOLIS Microplate System is a 4 plate fully integrated microplate processing system designed for use with multiple EIA assays.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0697-2016·2016-02-24

    Abbott's Compounding Pharmacy Recalls Sterile Compounded Products Due to Sterility Concerns

    Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, after FDA inspection found lack of sterility assurance.

    Product
    papaverine phentolamine prostaglandin; 18/0.6 mg/6 mcg/mL; 10 mL unit size, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Drugs)·D-0685-2016·2016-02-24

    Abbott's Compounding Pharmacy Recalls Sterile Methylcobalamine Due to Sterility Concerns

    Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile methylcobalamine injections because an FDA inspection found concerns regarding the assurance of sterility.

    Product
    methylcobalamine 10 mg/mL, 10 mL and 12 mL unit sizes, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
    Category
    Drug
    Distribution
    1 state