The Recall Desk

Severity 5 of 5

Critical recalls

Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.

What “critical” means here

Severity 5 (Critical) covers recalls where deaths or serious injuries have been reported, or where the agency itself classified the action as the highest severity (FDA Class I, NHTSA 'death/serious injury reported'). These are the recalls you should treat as urgent — stop using the product immediately and follow the agency's guidance. Common Severity-5 categories are pathogen-contaminated ready-to-eat foods (Listeria, E. coli O157, Salmonella), drug products with confirmed adverse-event reports, and vehicle defects with documented fatal crashes.

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.

6401–6425 of 7444

  • CriticalFDA (Food)·F-1462-2013·2013-06-05

    Whole Foods Peanut Butter Chocolate Chunk Cookies Recalled for Salmonella Risk

    The Sourdough: A European Bakery Inc. is recalling Whole Foods peanut butter chocolate chunk cookies because they were made with peanut butter recalled for salmonella.

    Product
    Whole Foods 3 oz Peanut Butter Chocolate Chunk Cookies sold under PLU 47963 from the retail store self-serve pastry case.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1461-2013·2013-06-05

    Whole Foods Peanut Butter Cookies Recalled Due to Salmonella Risk

    The Sourdough: A European Bakery Inc. is recalling Whole Foods 3 oz Peanut Butter Cookies because they were made with peanut butter recalled for salmonella.

    Product
    Whole Foods 3 oz Peanut Butter Cookies sold under PLU 47963 from the retail store self-serve pastry case.
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-1450-2013·2013-06-05

    Pecan Deluxe Peanut Butter Fudge Ribbon Recalled for Salmonella Risk

    Pecan Deluxe Candy Company is recalling Peanut Butter Fudge Ribbon because it was made with peanut butter previously recalled for salmonella.

    Product
    Peanut Butter Fudge Ribbon, 50 lb Pail, Item Number 07-094-50, Manufactured by Pecan Deluxe Candy Company, 2570 Lone Star Drive, Dallas, TX 75212
    Category
    Food
    Distribution
    12 states
  • CriticalFDA (Food)·F-1431-2013·2013-05-29

    Go Max Go Foods Recalls Vegan Peanut Butter Cups for Undeclared Milk

    Go Max Go Foods is recalling Cleo's Peanut Butter Cups because they contain undeclared milk despite being labeled as dairy-free.

    Product
    Cleo's Peanut Butter Cups creamy peanut butter in a rice-milk chocolately coating, 1.5 oz, gluten-free, dairy-free & vegan, no trans fats, nothing artificial. Distributed by Go Max Go Foods, LLC 40 Paseo Del Antiope, Santa Fe, NM 87506.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1447-2013·2013-05-29

    Whole Foods Peanut Sesame Noodles Recalled for Salmonella Risk

    Whole Foods Market is recalling Peanut Sesame Noodles distributed in Texas due to potential Salmonella contamination from Sunland, Inc. peanuts.

    Product
    Peanut Sesame Noodles Dist. by Whole Foods Market, UPC 222099604192
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1446-2013·2013-05-29

    Whole Foods Recalls Chicken Spring Rolls Due to Salmonella Risk

    Whole Foods Market is recalling Chicken Spring Rolls because they were manufactured with peanuts from Sunland, Inc., which may be contaminated with Salmonella.

    Product
    Chicken Spring Rolls Dist. by Whole Foods Market, UPC 225757203997
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1432-2013·2013-05-29

    Go Max Go Foods Recalls Vegan Candy Bars for Undeclared Milk

    Go Max Go Foods is recalling Jokerz vegan candy bars because they contain undeclared milk despite being labeled dairy-free.

    Product
    Jokerz Candy Bar peanuts, caramel, & nougat in a a rice-milk chocolately coating, 2.1 oz, dairy-free, vegan, no trans fats, nothing artificial. Distributed by Go Max Go Foods, LLC 40 Paseo Del Antilope, Santa Fe, NM 87506.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1442-2013·2013-05-29

    FDA Recalls Goldenbrook Farms Peanut Butter Bash Ice Cream Due to Salmonella Risk

    Brookshire Grocery Company is recalling Goldenbrook Farms Peanut Butter Bash Ice Cream because the peanut butter ingredient may be contaminated with Salmonella.

    Product
    Goldenbrook Farms Peanut Butter Bash Ice Cream, 1/2 gallon carton with UPC code 0009282530538
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-1433-2013·2013-05-29

    Go Max Go Foods Recalls Vegan Candy Bars for Undeclared Milk

    Go Max Go Foods is recalling Twilight Candy Bars labeled as dairy-free because they contain undeclared milk.

    Product
    Twilight Candy Bar caramel & chocolatey nougat in a a rice-milk chocolately coating, 2.1 oz, dairy-free, vegan, no trans fats, nothing artificial. Distributed by Go Max Go Foods, LLC 40 Paseo Del Antilope, Santa Fe, NM 87506.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1443-2013·2013-05-29

    Conagra Recalls Orville Redenbacher's Kettle Korn Popcorn for Undeclared Milk

    Conagra is recalling Orville Redenbacher's Classic Kettle Korn popcorn because it may contain undeclared milk, posing a health hazard to consumers with milk allergies.

    Product
    Orville Redenbacher's Classic Kettle Korn, sweet and salty popcorn, ready-to-eat, packaged in 5-oz/plastic bags (Unit UPC code 027000523216) and 1.5-oz/plastic bags (Unit UPC code 027000523254).
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-338-2013·2013-05-22

    Casanova Capsules Recalled for Undeclared Sildenafil and Tadalafil

    Performance Plus Marketing is recalling Casanova Capsules because they may contain undeclared sildenafil and tadalafil, making them unapproved drugs.

    Product
    CASANOVA Capsules, 450 mg, MALE SEXUAL ENHANCER, supplied i n1 count blister packs, UPC 736211906892; Distributed by: Casanova Distributors, Tucker, GA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-336-2013·2013-05-22

    FDA Recalls Mojo Nights Capsules for Unapproved Active Ingredients

    Performance Plus Marketing is recalling Mojo Nights Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.

    Product
    Mojo nights Capsules, Male Sexual Enhancer, supplied in 1 and 5 count blister packs, Distributed By: Mojo Health, Pompano Beach, FL I count blister UPC - 718122119738; 5 count blister UPC - 705105836430;
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-321-2013·2013-05-22

    Green Valley Drugs Recalls Methylprednisolone Injectable Suspension Due to Sterility Failure

    Green Valley Drugs is recalling Methylprednisolone Preservative Free 40 mg/mL injectable suspension because testing revealed positive sterility results.

    Product
    Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension, 1 mL Vials and 2 mL Vials and 1 mL pre-filled syringes, For Office Use Only, Manufactured by Green Valley Drugs, Henderson, NV.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-334-2013·2013-05-22

    FDA Recalls Blue Diamond Pill for Undeclared Sildenafil and Tadalafil

    Performance Plus Marketing, Inc. is recalling Blue Diamond Pill male sexual enhancement products because they may contain undeclared sildenafil, tadalafil, and analogues.

    Product
    BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution Los Angeles, CA 90026. 1 count blister: UPC 705105524764, 5 count blister: UPC 736211124012, 10 count blister: UPC 736211123916.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1275-2013·2013-05-22

    Cook Medical Recalls Zilver PTX Drug-Eluting Peripheral Stent

    Cook Medical is recalling Zilver PTX Drug-Eluting Peripheral Stents due to delivery system fractures and tip separations that resulted in one death.

    Product
    Zilver PTX Drug-Eluting Peripheral Stent, - 7 mm X 80mm; 125 cm, Rx, Sterile Product Usage: The Zilver PTX Drug -Eluting Peripheral Stent is a self expanding, small metal, mesh tube (stent) with the outer surface coated with the drug Paclitaxel that can be Implanted in an art
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-325-2013·2013-05-22

    FDA Recalls Unapproved ROCK-IT MAN Male Sexual Stimulant Capsules

    Consumer Concepts is recalling ROCK-IT MAN capsules because FDA analysis found they contain an unapproved sildenafil analogue.

    Product
    ROCK-IT MAN capsules, male sexual stimulant, packaged in 1-count (UPC 8 53447 02003 8) and 2-count (UPC 8 53447 00204 1) blister cards, Distributed by Consumer Concepts.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-335-2013·2013-05-22

    BLUE Diamond Platinum Capsules Recalled for Undeclared Active Ingredients

    Performance Plus Marketing is recalling BLUE Diamond Platinum Capsules because they may contain undeclared sildenafil, tadalafil, and analogues, making them unapproved drugs.

    Product
    BLUE Diamond PLATINUM Capsules, 1000 mg, supplied in 1, 5 and 10 count blister packs, Distributed By: DH Distribution Los Angeles, CA 90026 1 count blister UPC -608641933543; 5 count blister UPC - 608641932867; 10 count UPC -608641933536
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-322-2013·2013-05-22

    Green Valley Drugs Recalls Cyanocobalamin Injection Due to Sterility Failure

    Green Valley Drugs is recalling Cyanocobalamin 1000 mcg/mL injection because testing revealed positive sterility results.

    Product
    Cyanocobalamin 1000 mcg/ml, injection 30 mL, MDV, For Office Use Only, Green Valley Drugs, Manufactured by Green Valley Drugs, Henderson, NV.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-328-2013·2013-05-22

    Evol Nutrition Recalls Mojo Nights for Her Due to Unapproved Ingredients

    Evol Nutrition is recalling Mojo Nights for Her capsules because they contain unapproved ingredients used to treat male erectile dysfunction.

    Product
    Mojo Nights for Her, 1 capsule, UPC 7 18122 12133 5, Distributed By: Mojo Health Lauderhill, FL 33351
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1274-2013·2013-05-22

    Cook Medical Recalls Zilver PTX Drug-Eluting Peripheral Stent Due to Catheter Fracture

    Cook Medical is recalling Zilver PTX Drug-Eluting Peripheral Stents because the delivery system's inner catheter can fracture or separate after deployment, a defect linked to one reported death.

    Product
    Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm; 125 cm, Rx, Sterile Product Usage: The Zilver PTX Drug -Eluting Peripheral Stent is a self expanding, small metal, mesh tube (stent) with the outer surface coated with the drug Paclitaxel that can be Implanted in an ar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1371-2013·2013-05-08

    DZH Import Recalls Dried Mushrooms for Undeclared Sulfites

    DZH Import & Export Inc. is recalling two brands of dried mushrooms sold in New York City because they contain undeclared sulfites.

    Product
    Dried mushrooms sold under the following brand names: 1) CURIOSITY OF DASHAN brand DRIED MUSHROOM, N.W. 100G (3.5 OZ), UPC 6 939457 003484, Product of China --- Imported By: DZH Import & Export Inc. 70-21 51 Avenue, Woodside, NY 11377 Tel: 718-205-8312 Fax: 718-205-8146 --
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-1369-2013·2013-05-08

    Farm Rich Pizza Dippers Recalled Due to E. coli O121 Contamination

    Rich Products Corp is recalling Farm Rich Better For You Pizza Dippers nationwide due to potential E. coli O121 contamination.

    Product
    Farm Rich Better For You Pizza Dippers-Pizza Dough made with Whole Wheat Flour and Stuffed with Mozzarella Cheese and Reduced Fat Mozzarella Cheese, Net Wt. 27-LBS (10 X 2.7-LB), UPC Code 00041322652782, Product Code 65278.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1170-2013·2013-05-08

    Hospira Recalls GemStar Infusion Pumps Due to Unexpected Shutdowns

    Hospira Inc. is recalling GemStar infusion pumps because they may shut off during use without warning, potentially interrupting patient medication delivery.

    Product
    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two disposab
    Category
    Medical Device
    Distribution
    Distributed nationwide