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.

17151–17175 of 29206

  • SevereFDA (Food)·F-0691-2017·2016-12-21

    Back to Nature Mini Chocolate Chunk Cookies Recalled for Undeclared Milk

    Back to Nature Foods is recalling specific lots of Mini Chocolate Chunk Cookies because they contain undeclared milk, a major food allergen.

    Product
    Back to Nature Mini Chocolate Chunk Cookies, 6 - 1.25oz (35g) UPC 8-19898-01114-8 (tray) and UPC 8-19898-01115-5 (pouch); 100 - 1.25oz (35g) UPC 8-19898-01148-3 (case) and UPC 8-19898-01115-5 (pouch), 50 - 2.5oz (70g) UPC 8-19898-01139-1 (case) and UPC 8-19898-01143-8 (pouch)…
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Food)·F-0742-2017·2016-12-21

    Cargill Recalls Liquid Butter Alternative for Excessive Additives

    Cargill is recalling Beyond Premium Liquid Butter Alternative due to excessive amounts of TBHQ and dimethyl polysiloxane.

    Product
    Beyond PREMIUM LIQUID BUTTER ALTERNATIVE ,ARTIFICIALLY FLAVORED SODIUM FREE, NET/NETO 1 GAL (3.79 L) INGREDIENTS; SOYBEAN OIL, HYDROGENATED SOYBEAN OIL ***TBHQ***DIMETHYLPOLYSILOXANE ***CONTAINS: SOY. UPC 7 58108 08439 1
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Food)·F-0703-2017·2016-12-21

    First Source Recalls Hikers Haven Trail Mix for Listeria Risk

    First Source LLC is recalling Hikers Haven Trail Mix due to potential Listeria monocytogenes contamination. The product was distributed in 11 states.

    Product
    Flave! HIKERS HAVEN TRAIL MIX, Net Wt. 21.5 OZ (1 LB 5.5 OZ) 609g, packed 12 per case
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0187-2017·2016-12-21

    Cantrell Drug Recalls Calcium Chloride Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling 645 vials of Calcium Chloride Injection Solution because the firm cannot assure the sterility of the product.

    Product
    Calcium Chloride, (1 g/10 mL) Injection Solution 10 mL, 10% Single-Dose Vial, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0199-2017·2016-12-21

    Cantrell Drug Recalls Morphine Sulfate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 1,748 bags of Morphine Sulfate 1 mg/mL due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Morphine Sulfate 1 mg/mL in 0.9% Sodium Chloride, 100 mL Bag, Single-Dose Bag, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-160-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0673-2017·2016-12-21

    RL Schreiber Demi-Glace Brown Sauce Mix Recalled for E. Coli Risk

    RL Schreiber Inc is recalling Demi-Glace Brown Sauce Mix because it was manufactured with flour potentially contaminated with E. coli.

    Product
    R.L. SCHREIBER Demi-Glace Brown Sauce Mix 18 oz (510 G)white plastic bag INGREDIENTS: Enriched Bleached Wheat Flour***CONTAINS: Wheat, Soy, Milk Produced in a facility with Egg
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0319-2017·2016-12-21

    Hickory Harvest Rucker's Cajun Mix Recalled for Listeria Contamination

    Ohio Hickory Harvest Brand Products Inc. is recalling 25 lb. bags of Rucker's Cajun Mix due to potential Listeria monocytogenes contamination.

    Product
    Hickory Harvest FOODS Rucker's Cajun Mix 25 lb. bag in a box INGREDIENTS: Cajun Sesame Sticks***soybean oil***Sunflower Kernels, Hot & Spicy Peanuts***Contains: Peanut, Soy, Wheat.
    Category
    Food
    Distribution
    43 states
  • SevereFDA (Drugs)·D-0195-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 935 vials of Hydromorphone HCl 50 mg/50 mL single-dose syringes due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0750-2017·2016-12-21

    LSG Sky Chefs Recalls Mediterranean Chicken Sandwiches for Listeria Risk

    LSG Sky Chefs is recalling FRESH TO GO Mediterranean Chicken with Hummus sandwiches due to potential Listeria monocytogenes contamination from a recalled hummus ingredient.

    Product
    FRESH TO GO Mediterranean Chicken with Hummus sandwich, close-face ready-to-eat sandwich, refrigerated, packed in plastic clam shell, net wt. 8 oz. The UPC is 0 52548 58888 5.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0184-2017·2016-12-21

    Cantrell Drug Recalls Calcium Chloride Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 80 bags of Calcium Chloride 1 g/50 mL due to a lack of assurance of sterility.

    Product
    Calcium Chloride 1 g/50 mL* Added to 5% Dextrose (20 mg/mL)*, Single-Dose Bag, Rx Only, Hospital/Office Use Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-175-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0185-2017·2016-12-21

    Cantrell Drug Company Recalls Phenylephrine HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 30,796 syringes of Phenylephrine HCl 1 mg/10 mL due to a lack of assurance of sterility. The recall covers products distributed nationwide.

    Product
    Phenylephrine HCl 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL Single-Dose Syringe, Rx Only Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-171-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0200-2017·2016-12-21

    Cantrell Drug Recalls Neostigmine Methylsulfate Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Neostigmine Methylsulfate injection syringes because the firm cannot ensure the products are sterile.

    Product
    Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) Single-Dose Syringe, For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-046-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0201-2017·2016-12-21

    Cantrell Drug Company Recalls Oxytocin Injection Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 2,681 bags of Oxytocin 30 USP Units due to a lack of assurance of sterility. The affected product is distributed nationwide.

    Product
    Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag, Single-Dose Bag, Injection Solution for IV Use Only, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-056-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0693-2017·2016-12-21

    Mary's Homemade Vegetable Soup Recalled for Botulism Risk

    Mary's Homemade Vegetable Soup is being recalled because it is underprocessed and may pose a Clostridium Botulinum hazard.

    Product
    Mary's Home Made Vegetable Soup; 16 FL. OZ. (1 Pint) OR 32 FL. OZ. (1 Quart); Heat and Serve
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0197-2017·2016-12-21

    Cantrell Drug Recalls Lidocaine HCl Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 162 syringes of Lidocaine HCl 1% because the firm cannot assure the sterility of the product.

    Product
    Lidocaine HCl 1%, 10 mL Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0692-2017·2016-12-21

    Green Cuisine Recalls Pesto Pasta Salad Due to Listeria Risk

    Green Cuisine, Inc. is recalling Pesto Pasta Salad with Arugula because it may be contaminated with Listeria monocytogenes.

    Product
    Pesto Pasta Salad with Arugula, Net Wt. 16oz, UPC 857898004333
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0707-2017·2016-12-21

    Troyer Cheese Recalls Peanut Butter Pretzels for Listeria Risk

    Troyer Cheese Inc is recalling Backroad Country Peanut Butter Pretzels due to potential Listeria monocytogenes contamination. The product was distributed to 26 states.

    Product
    BACKROAD COUNTRY PEANUT BUTTER PRETZELS, Net Wt. 7 oz (198g) Product Code 15372 BEST IF USED BY 05/2017
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0700-2017·2016-12-21

    First Source Recalls Oriental Snack Mix for Listeria Risk

    First Source LLC is recalling specific lots of Oriental Snack Mix due to potential Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.

    Product
    Oriental Snack Mix under the following labels: 1) Flave! ORIENTAL MIX, NET WT 6OZ (170g), shipped 12 packs per case, 2) Alpine Valley Oriental Snack Mix, 4oz 3) 15 LB Bulk ALPINE VALLEY ORIENTAL DELIGHT MIX, shipped 1 per case
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Drugs)·D-0196-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Injection Vials Due to Sterility Concerns

    Cantrell Drug Company is recalling 93 vials of Hydromorphone HCl injection solution nationwide due to a lack of assurance of sterility.

    Product
    Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0694-2017·2016-12-21

    First Source LLC Recalls Fitness Mix for Listeria Contamination Risk

    First Source LLC is recalling multiple varieties of Fitness Mix due to the potential for Listeria monocytogenes contamination. The product was distributed to retail stores in 11 states.

    Product
    FITNESS MIX sold under the following labels: 1) 15 LBS ALPINE VALLEY FITNESS MIX, packed as 1 per case, 2) Wegmans square tub FITNESS MIX, 20 oz, packed as 12 per case, Flave! FITNESS MIX, NET WT 8OZ (226g), packed as 12 per case, 4) FITNESS MIX, NET WT 5 OZ (141g), shipped 6…
    Category
    Food
    Distribution
    11 states
  • SevereFDA (Food)·F-0733-2017·2016-12-21

    Publix Danish Maple Walnut Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Maple Walnut Coffee Cake strips due to the presence of small metal shavings.

    Product
    Publix Danish Maple Walnut Coffee Cake Strip, 14 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0186-2017·2016-12-21

    Cantrell Drug Company Recalls Calcium Chloride Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 73 bags of Calcium Chloride in 0.9% Sodium Chloride due to a lack of assurance of sterility.

    Product
    Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag, Rx Only, Single-Dose Bag Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-102-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0204-2017·2016-12-21

    Cantrell Recalls Succinylcholine Chloride Injection Due to Sterility Concerns

    Cantrell Drug Company is recalling specific lots of Succinylcholine Chloride 200 mg/10 mL injection syringes because the firm cannot ensure the products are sterile.

    Product
    Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL (20 mg/mL) ,Single-Dose Syringe Injection Solution, For Slow IV Use Only ,Rx Only, Cantrell Drug Company 7321 Cantrell Rd Little Rock, AR 72207, NDC 52533-067-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0203-2017·2016-12-21

    Cantrell Drug Recalls Ropivacaine HCl Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.

    Product
    Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-185-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V913000·2016-12-20

    Volkswagen Recalls 2009-2010 Models for ABS Control Unit Failure

    Volkswagen is recalling 2009-2010 Jetta, GTI, Golf, and Audi A3 vehicles because the ABS control unit may fail, potentially causing loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI JETTA, GTI, GOLF, EOS
    Category
    Vehicle
    Distribution
    Distributed nationwide