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.

33426–33450 of 50502

  • HighFDA (Food)·F-1104-2017·2017-01-18

    Piazza Produce Recalls Quebec Chicken Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Quebec Chicken seasoning in various sizes because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Quebec Chicken seasoning, 1.25 lb plastic jar, product number 67688; Quebec Chicken seasoning, 5 lb plastic gallon, product number 67707; Quebec Chicken seasoning, 10 lb plastic pail, product number 67726
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0872-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes because they lack adequate labeling, including undeclared wheat, walnut, pine nuts, pumpkin seeds, and sesame.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Black Truffles with Five Nuts. Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1100-2017·2017-01-18

    Piazza Produce Recalls Jamaican Jerk Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Jamaican Jerk seasoning in various sizes because the product labeling does not list ingredients, including undeclared soybean oil.

    Product
    Jamaican Jerk seasoning 6.25 lb plastic gallon, product number 64838; Jamaican Jerk seasoning, 1.75 lb plastic jar, product number 64819; Jamaican Jerk seasoning, 12 lb plastic pail, product number 64857
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1219-2017·2017-01-18

    Stonewall Kitchen Toasted Coconut Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling Toasted Coconut Pancake & Waffle Mix due to potential salmonella contamination. Consumers should not consume the product.

    Product
    Stonewall Kitchen Toasted Coconut Pancake & Waffle Mix, Packaged in a 16oz. canister UPC: 711381033494 Item #: 551133
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0871-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Wheat Allergen

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes because the products lack adequate labeling, including undeclared wheat.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Wolfberry & Dates Paste. Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighCPSC·17728·2017-01-12

    Nantucket Distributing Recalls Pre-Lit Christmas Trees Due to Fire Hazard

    Nantucket Distributing is recalling pre-lit artificial Christmas trees because the fuse can overheat and blow, posing a fire hazard. No injuries have been reported.

    Product
    Pre-Lit Globe Light Christmas trees
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17726·2017-01-12

    BRP Recalls Side-by-Side Off-Road Vehicles Due to Roll-Away Hazard

    BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V033000·2017-01-12

    GM Recalls 2016-2017 Chevrolet Suburban HD for Incorrect Rearview Mirror

    General Motors is recalling 2016-2017 Chevrolet Suburban HD vehicles equipped with a convex right-hand outside mirror instead of a non-convex one, which may cause drivers to misjudge distance.

    Product
    CHEVROLET — CHEVROLET SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17068·2017-01-12

    Boosted Recalls Electric Skateboards Due to Fire Hazard

    Boosted Inc. is recalling 2nd Generation Dual+ electric skateboards because the lithium ion battery packs can overheat and smoke, posing a fire hazard.

    Product
    Electric-powered skateboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0269-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Lipo-C Vials Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 69 vials of Lipo-C compounded between May and November 2016 because the agency could not ensure the products were sterile.

    Product
    Lipo-C (Methionine 25 mg/Inositol 50 mg/Choline Chloride 50 mg/Carnitine (L) 100 mg/Methylcobalamin 1 mg/Thiamine HCL 50 mg/Rivoflavin-5-Phosphate Sod 5 mg/Niacinamide 50 mg/Dexpanthenol 5 mg/Pyridoxine HCL 1.25 mg/Lidocaine HCL 10 mg/mL), (30 ML). Compounded by Tri-Coast…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0351-2017·2017-01-11

    Wells Pharmacy Recalls Compounded Chorionic Gonadotropin Injectable Kits

    Wells Pharmacy Network LLC is recalling 908 compounded Chorionic Gonadotropin Injectable Kits nationwide due to a lack of assurance of sterility.

    Product
    Chorionic Gonadotropin Lyophilized, 20,000 unit Injectable Kit, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0942-2017·2017-01-11

    Pride Mobility Recalls TRU-Balance 3 Power Positioning Systems

    Pride Mobility Products Corp is recalling 12,343 TRU-Balance 3 Power Positioning Systems because the back and tilt base can separate when tilted beyond the specified angle.

    Product
    TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0946-2017·2017-01-11

    Smith & Nephew Recalls Modular Hip Prosthesis Necks Due to Adverse Events

    Smith & Nephew is recalling 13,671 modular neck hip prostheses due to a higher than anticipated complaint and adverse event trend.

    Product
    Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0319-2017·2017-01-11

    Tri-Coast Pharmacy Recalls TriMix Injection Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 17 vials of TriMix injection because the agency could not ensure the products were sterile.

    Product
    TriMix, Alprostadil/Phentolamine/Papaverine 40mcg/2mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0945-2017·2017-01-11

    Smith & Nephew Recalls Modular SMF Hip Prostheses Due to Adverse Events

    Smith & Nephew is recalling Modular SMF and Modular REDAPT Hip Systems due to a higher-than-anticipated trend in complaints and adverse events.

    Product
    Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1168-2017·2017-01-11

    Elmec Caramel Bread Pudin Recalled for Undeclared Wheat and Soy Allergens

    Elmec Industries is recalling approximately 84,000 units of Caramel Bread Pudin sold in Puerto Rico due to undeclared wheat and soy allergens.

    Product
    Pudin es Cedo***Homestyle Caramel Bread Pudin***Ready to Eat***Hecho en Puerto Rico***Serving Size 3 oz (85g)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1161-2017·2017-01-11

    Tipiak Pearled Couscous Recalled for Potential Foreign Metal Fragments

    Tipiak Inc is recalling specific lots of Pearled Couscous due to the potential presence of foreign metal fragments.

    Product
    Tipiak Pearled Couscous Easy cooking 12.3 Oz (350g) Item Number: 10020450803 Product of France
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0944-2017·2017-01-11

    Smith & Nephew Recalls Modular REDAPT Hip Systems Due to Adverse Events

    Smith & Nephew is recalling 6,266 units of Modular REDAPT and Modular SMF Hip Systems worldwide due to a higher than anticipated complaint and adverse event trend.

    Product
    Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0332-2017·2017-01-11

    Wells Pharmacy Recalls MIC Combo Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling MIC Combo injectable vials because the agency could not ensure the product was sterile.

    Product
    MIC Combo - Standard 15 mg/50 mg/100 mg/mL Injectable, 30 mL vials, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0372-2017·2017-01-11

    Wells Pharmacy Recalls Injectable Compound Due to Sterility Assurance Concerns

    Wells Pharmacy Network LLC is recalling 1,716 vials of a compounded injectable product nationwide due to a lack of assurance of sterility.

    Product
    MIC/B-COMP+CARN+LIDO, 15 mg/30 mg/30 mg/85 mg/20 mg/mL Injectable, 30 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·17725·2017-01-11

    Linon Home Décor Recalls Cynthia Dressers Due to Tip-Over Hazard

    Linon Home Décor is recalling Cynthia dressers sold at Wayfair.com because they can tip over if not anchored, posing a risk of death or injury to children.

    Product
    Cynthia dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide