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.

32601–32625 of 50502

  • HighFDA (Food)·F-1876-2017·2017-04-12

    IKEA Recalls Chocolate Wafers for Undeclared Hazelnut and Almond

    IKEA is recalling Godis Chokladran chocolate wafers because the packaging fails to declare hazelnut and almond ingredients, posing a risk to consumers with allergies.

    Product
    Godis Chokladran Wafers filled and covered with Milk chocolate; Net Wt 5.9 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-1751-2017·2017-04-12

    Philips BrightView XCT Gamma Cameras Recalled for Brake Hub Assembly Error

    Philips is recalling 90 BrightView XCT gamma cameras because a brake hub assembly error can cause the detector to backdrive.

    Product
    BrightView XCT model number 882482 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated, and…
    Category
    Medical Device
    Distribution
    29 states
  • HighCPSC·17130·2017-04-12

    Customatic Recalls Adjustable Beds Due to Electric Shock Hazard

    Customatic Beds is recalling about 50,000 adjustable bed bases because side-mounted AC outlets may be incorrectly wired, posing an electric shock hazard.

    Product
    Adjustable beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1874-2017·2017-04-12

    IKEA Recalls Chocolate Squares for Undeclared Milk, Almond, and Hazelnut

    IKEA is recalling Choklad Lingon & Blabar chocolate squares due to undeclared milk, almond, and hazelnut ingredients.

    Product
    Choklad Lingon & Blabar Assortment of milk chocolate Squares with lingonberry pieces and dark chocolate squares with bilberry pieces; Net Wt 6.3 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1837-2017·2017-04-12

    Kwei Chow Mustard Strip Recalled for Undeclared Wheat Allergen

    Kwei Chow Sauce Industry Co., Ltd. is recalling 8,488 jars of Mustard Strip with chili in oil because the product contains undeclared wheat.

    Product
    Kwei Chow brand Mustard Strip with chili in oil, net weight 7.05 Oz, sauce in glass jars, shelf stable
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1826-2017·2017-04-12

    Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars Recalled for Almond Mislabeling

    Nestle USA is recalling Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars because two consumers found almond bars in the packaging. The product was distributed in eight states and Washington, D.C.

    Product
    Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars; 3 - 3 FL oz.. bars (9 FL ox (266 ml)
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1730-2017·2017-04-12

    Centurion Medical Recalls Post-Op Eye Trays Due to Sterile Packaging Breach

    Centurion Medical Products is recalling 476 Post-Op Eye Trays because the sterile eye pads inside may have had a packaging breach.

    Product
    POST-OP EYE TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1735-2017·2017-04-12

    Centurion Convenience Kits Recalled Due to Potential Sterile Packaging Breach

    Centurion Medical Products is recalling 1,692 Convenience Kits containing eye pads due to a potential breach in sterile packaging.

    Product
    OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Food)·F-1835-2017·2017-04-12

    Kwei Chow Prime Spicy Pot Paste Recalled for Undeclared Wheat

    Kwei Chow Sauce Industry Co., Ltd. is recalling Prime Spicy Pot Paste because the product contains undeclared wheat, a major food allergen.

    Product
    Kwei Chow brand Prime Spicy Pot Paste, net weight 7.10 Oz, sauce in glass jars, shelf stable
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1875-2017·2017-04-12

    IKEA Recalls Chocolate Products Due to Undeclared Milk, Almond, and Hazelnut

    IKEA is recalling specific chocolate products, including Godis Chokladkrokant, due to undeclared milk, almond, and hazelnut ingredients.

    Product
    Godis Chokladkrokant Milk chocolate with butterscotch pieces; Net Wt 15.9 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sweden.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Food)·F-1861-2017·2017-04-12

    Amish Bakery Chocolate Chip Bar Recalled for Missing Soy Label

    Original Amish Bakery LLC is recalling Chocolate Chip Grand-ola Bars because the label failed to list soy as an ingredient.

    Product
    Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT. 2.8 OZ (80g) UPC 0 14757 13000 2 Contains: Wheat, Tree Nuts, Dairy Ingredients: Oats, chocolate chips (sugar,chocolate liquor, cocoa butter, whole milk, lecithin [an emulsifier], salt, vanilla), brown sugar, wheat, corn…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1743-2017·2017-04-12

    Sterile Saline Dressing Recalled Due to Compromised Sterility Barrier

    FDA is recalling Kerlix Super Sponge Saline Dressings because the sterile barrier is breached, potentially compromising sterility.

    Product
    Covidien Kerlix Super Sponge Saline Dressing, Sterile Item Code: 3338 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic debridement process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1732-2017·2017-04-12

    Centurion Convenience Kits Recalled for Potential Sterile Packaging Breach

    Centurion Medical Products is recalling 588 Convenience Kits containing Curity Oval Eye Pads due to a potential breach in sterile packaging.

    Product
    OPHTHALMIC DRS TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-1750-2017·2017-04-12

    Philips Recalls 84 BrightView SPECT Gamma Cameras Due to Brake Hub Defect

    Philips is recalling 84 BrightView SPECT gamma cameras because a brake hub assembly error can cause the detector to backdrive.

    Product
    BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated…
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-1742-2017·2017-04-12

    Recall of Sterile Wound Dressings Due to Compromised Sterility Barrier

    Covidien is recalling Curity Wet Dressings because the sterile barrier was breached, potentially compromising sterility. The recall affects units distributed worldwide.

    Product
    Covidien Curity Wet Dressing 8 x 4 (20.3 cm x 10.2 cm), Sterile Item Code: 3337 Curity sodium chloride dressing is saturated in a 20% hypertonic saline solution. The dressing is designed to help promote biological cleansing within the wound and aid in the autolytic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2017·2017-04-12

    BD Vacutainer Blood Collection Tubes Recalled for Stopper Pullout Risk

    Becton Dickinson is recalling specific lots of BD Vacutainer Buffered Sodium Citrate blood collection tubes because stoppers may pull out during use.

    Product
    BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes, 4.5 mL, 13 x 75 mm, Mfd: Becton Dickinson and Company Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection Tube that provides means of collecting, transporting and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1740-2017·2017-04-12

    Recall of Sterile Eye Pads Due to Compromised Sterility Barrier

    Covidien LLC is recalling Curity Eye Pads because the sterile barrier was breached, potentially compromising sterility.

    Product
    Covidien Curity Eye Pad Oval, 1-5/8 x 2-5/8 (4.2 cm x 6.7 cm), Sterile Item Code: 2841 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1734-2017·2017-04-12

    Centurion Medical Recalls Post-Operative Ophthalmic Dressing Kits Due to Sterility Concerns

    Centurion Medical Products is recalling 45 post-operative ophthalmic dressing kits because the eye pads inside may have had a breach in sterile packaging.

    Product
    POST-OPERATIVE OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
    Category
    Medical Device
    Distribution
    9 states
  • HighCPSC·17739·2017-04-11

    John Deere Recalls Gator Utility Vehicles Due to Crash Hazard

    John Deere is recalling about 8,500 Gator Utility Vehicles because a loose dust boot on the throttle cable can prevent the vehicle from stopping, posing a crash hazard.

    Product
    Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V246000·2017-04-11

    Mercedes-Benz Recalls 2016-2017 E300 Vehicles for Spoiler Defect

    Mercedes-Benz is recalling 2016-2017 E300 and E300 4MATIC vehicles because the roof-mounted spoiler may detach while driving, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17129·2017-04-11

    Anaheim and Moen Recall Garbage Disposals Due to Impact Hazard

    Anaheim Manufacturing and Moen are recalling about 146,000 garbage disposals because a metal component can break off and exit the unit, posing an impact hazard.

    Product
    Garbage disposals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17128·2017-04-11

    Teavana Recalls Flip Tumblers Due to Hot Liquid Burn Hazard

    Starbucks is recalling Teavana Flip Tumblers because they can leak hot liquid, posing a burn risk. Consumers should stop using them and contact Starbucks for a refund.

    Product
    Teavana Flip Tumblers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V239000·2017-04-10

    Thor Motor Coach Recalls 2017 Motorhomes Due to Incorrect Hitch Weight Labels

    Thor Motor Coach is recalling 2017 Ace, Hurricane, and Windsport motorhomes because tow hitch labels incorrectly state a 10,000 lb capacity instead of the actual 8,000 lbs.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR ACE, WINDSPORT, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide