The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

17126–17150 of 29206

  • SevereNHTSA·16V925000·2016-12-22

    Ford Recalls 2016-2017 Vehicles for Turbocharger Oil Leak Fire Risk

    Ford is recalling specific 2016-2017 Taurus, Flex, MKT, and Explorer vehicles because improperly brazed turbocharger tubes may leak oil, increasing fire risk.

    Product
    FORD — FORD, LINCOLN FLEX, TAURUS, MKT, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2016·2016-12-22

    Pork Rinds & Snacks Recalls Pork Skin Products Due to Salmonella Risk

    Pork Rinds & Snacks, LLC is recalling approximately 7,629 pounds of pork skin products that may be contaminated with Salmonella. The recall affects products shipped to five southeastern states.

    Product
    Pork Rinds & Snacks, LLC Recalls Pork Skin Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V926000·2016-12-22

    KME Predator Aerial Vehicles Recalled for Brake Defect

    KME is recalling certain Predator SS Aerial and Predator Aerial vehicles because rear brakes may engage without the pedal being pressed, increasing crash and fire risk.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V928000·2016-12-22

    Volvo Recalls 2013-2017 Trucks Due to Brake System Contamination Risk

    Volvo is recalling certain 2013-2017 VNL, VNM, and 2017 VNX trucks because incorrect software may allow oil and water to contaminate the brake system, potentially affecting braking performance.

    Product
    VOLVO — VOLVO VNM, VNX, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V927000·2016-12-22

    Volvo Recalls 2017 Trucks Due to Front Wheel Hub Defect

    Volvo is recalling 2017 VHD, VNL, and VNM trucks because front wheel hubs may fail, risking loss of vehicle control.

    Product
    VOLVO — VOLVO VNM, VNL, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V947000·2016-12-22

    Chrysler Recalls 2009 Durango, Aspen, and 2010 RAM 3500 for Air Bag Defect

    Chrysler is recalling specific 2009 Dodge Durango, Chrysler Aspen, and 2010 RAM 3500 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury.

    Product
    DODGE — DODGE, CHRYSLER DURANGO, redundant RAM 3500, ASPEN, RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0189-2017·2016-12-21

    Cantrell Drug Company Recalls Fentanyl Citrate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling Fentanyl Citrate bags due to a lack of assurance of sterility. The recall affects 2,545 bags distributed nationwide.

    Product
    Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0194-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 2,509 single-dose Hydromorphone HCl syringes nationwide due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-002-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0202-2017·2016-12-21

    Cantrell Drug Recalls Rocuronium Bromide Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 5,067 syringes of Rocuronium Bromide 50 mg/5 mL injection solution nationwide due to a lack of assurance of sterility.

    Product
    Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0188-2017·2016-12-21

    Cantrell Drug Recalls Fentanyl Citrate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 471 bags of Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0697-2017·2016-12-21

    First Source Recalls Sunflower Kernels for Listeria Contamination Risk

    First Source LLC is recalling specific lots of roasted and unsalted sunflower kernels due to potential Listeria monocytogenes contamination.

    Product
    ROASTED & UNSALTED SUNFLOWER KERNELS sold under the following labels: 1) ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 2) Tops square tub ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 3) EARTH FARE ROASTED & UNSALTED…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0706-2017·2016-12-21

    Troyer Cheese Recalls Backroad Country Honey Island Crunch Mix for Listeria Risk

    Troyer Cheese Inc is recalling Backroad Country Honey Island Crunch Mix due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.

    Product
    BACKROAD COUNTRY HONEY ISLAND CRUNCH MIX ,Net Wt. 9 oz (256g) Product Code 15356 BEST IF USED BY 05/2017
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0702-2017·2016-12-21

    First Source Recalls Flave! Beach Retreat Trail Mix for Listeria Risk

    First Source LLC is recalling Flave! Beach Retreat Trail Mix due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.

    Product
    Flave! BEACH RETREAT TRAIL MIX, Net Wt. 18.5 OZ (1 LB 2.5 OZ) 524g, packed 12 per case
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0191-2017·2016-12-21

    Cantrell Drug Recalls Glycopyrrolate Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Glycopyrrolate injection because the firm cannot assure the sterility of the product.

    Product
    Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL Single-Dose Syringe, For IV Use, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-028-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0709-2017·2016-12-21

    Troyer Cheese Recalls Sunflower Seeds for Listeria Risk

    Troyer Cheese Inc is recalling 30 lb bags of Backroad Country Roasted and Salted Sunflower Seeds due to potential Listeria monocytogenes contamination.

    Product
    BACKROAD COUNTRY ROASTED AND SALTED SUNFLOWER SEEDS ,Net Wt. 30 lb bag, UPC 1 13671 02091 5 Product Code 15318 BEST IF USED BY 05/2017
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Drugs)·D-0192-2017·2016-12-21

    Cantrell Drug Recalls Heparin Sodium Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 1,494 syringes of Heparin Sodium due to a lack of assurance of sterility. The products were distributed nationwide.

    Product
    Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0193-2017·2016-12-21

    Cantrell Drug Recalls Heparin Sodium Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 150 bags of Heparin Sodium 5,000 USP Units in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0698-2017·2016-12-21

    First Source Recalls Cranberry Delight Products for Listeria Risk

    First Source LLC is recalling various Sunshine Cranberry Delight products due to potential contamination with Listeria monocytogenes.

    Product
    SUNSHINE CRANBERRY DELIGHT sold under the following labels: 1) Wegmans square tub SUNSHINE CRANBERRY DELIGHT, 20 oz, shipped 12 packs per case, 2) 15 LBS ALPINE VALLEY SUNSHINE CRANBERRY DELIGHT, shipped 1 per case, 3) SUNSHINE CRANBERRY DELITE, NET WT 4.5 OZ (127g) shipped 6…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0318-2017·2016-12-21

    Big Y Cranberry Nut Trail Mix Recalled for Listeria Contamination

    Big Y cranberry nut trail mix is being recalled because it may be contaminated with Listeria monocytogenes. The product was distributed to 43 states.

    Product
    Big Y cranberry nut trail mix in plastic tub NET WT 20 OZ (1 LB 4 OZ) 567g INGREDIENTS: CRANBERRIES***PEANUTS, PEANUT OIL, RAISINS, SUNFLOWER KERNELS, PEPITAS, WALNUTS. CONTAINS: PEANUTS, WALNUTS UPC 0 18894 00457 8 DISTRIBUTED BY BIG Y FOODS, INC., SPRINGFIELD, ma 01104
    Category
    Food
    Distribution
    43 states
  • SevereNHTSA·16V922000·2016-12-21

    GM Recalls 2016 Buick Envision for Brake Line Cracking Risk

    General Motors is recalling 2016 Buick Envision vehicles because master cylinder brake lines may crack and leak fluid, potentially reducing braking performance.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0316-2017·2016-12-21

    Hickory Harvest Trail Mix Recalled for Listeria Contamination Risk

    Ohio Hickory Harvest Brand Products Inc. is recalling Sweet & Salty Trail Mix because it may be contaminated with Listeria monocytogenes.

    Product
    Hickory Harvest FOODS Sweet & Salty Trail Mix 25 lb. UPC 0-36232-00510-0, 4.5oz UPC 0-36232-06075-5. INGREDIENTS: Peanuts, Raisins***Sunflower Kernel*** AKRON, OH 44319 UPC 0 36232 00510 0
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Food)·F-0696-2017·2016-12-21

    First Source Recalls Sunflower Kernels for Listeria Contamination Risk

    First Source LLC is recalling specific lots of roasted and salted sunflower kernels due to potential Listeria monocytogenes contamination.

    Product
    ROASTED & SALTED SUNFLOWER KERNELS sold under the following labels: 1) ROASTED & SALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 2) Tops square tub ROASTED & SALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 3) EARTH FARE ROASTED & SALTED SUNFLOWER…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0190-2017·2016-12-21

    Cantrell Drug Company Recalls Fentanyl and Bupivacaine Bags for Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Fentanyl Citrate and Bupivacaine HCl bags due to a lack of assurance of sterility.

    Product
    Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium Chloride, 100 mL* Bag, Epidural Use Only, Single-Dose Bag, Hospital/Office Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-080-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0198-2017·2016-12-21

    Cantrell Drug Recalls Midazolam HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 37 syringes of Midazolam HCl 50 mg/50 mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL), Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-001-04
    Category
    Drug
    Distribution
    Distributed nationwide