The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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20401–20425 of 39660

  • SevereFDA (Drugs)·D-0878-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Magnesium Sulfate Injectable Bags

    SCA Pharmaceuticals is recalling 40 bags of Magnesium Sulfate injectable solution due to seam leaks that compromise sterility.

    Product
    MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable, 4g, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0737-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0875-2017·2017-06-07

    SCA Pharmaceuticals Recalls Hydrocodone Injectable Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 87 bags of Hydromorphone HCL injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml, Total Volume 100mL, Single Dose Container bag, (Total HYDROmorphone Dose 20 mg per 100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0300-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Cefazolin Sodium Injectable Bags

    SCA Pharmaceuticals is recalling 240 bags of cefazolin sodium injectable due to seam leaks that compromise sterility.

    Product
    ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g, Total Approximate Volume 100 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0522-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0872-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Seam Leaks

    SCA Pharmaceuticals is recalling 118 bags of fentanyl injection due to seam leaks that compromise sterility. The product was distributed nationwide in the USA.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0229-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2291-2017·2017-06-07

    MusclMasster Recalls Al-Er-G Capsules Containing Banned Ephedra Ingredient

    MusclMasster, LLC is recalling Al-Er-G Capsules because they contain ephedra herb, an ingredient banned by the FDA.

    Product
    The Green Herb 100% Natural AL-ER-G, 60 and 150 Capsules, Dietary supplement, This item is packed in a white bottle with a white cap. Each bottle contains 60 or 150 capsules, each capsule is 180 mg of ephedra herb in a 650 mg capsule. Batch#1892; product# 314.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0873-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 370 bags of fentanyl injection solution because the bags were leaking at the seam, compromising sterility.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0202-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V365000·2017-06-05

    Hyundai Recalls 2017 Santa Fe Sport for Seat Belt Anchor Defect

    Hyundai is recalling 2017 Santa Fe Sport vehicles because the driver's seat belt anchor bolt may not be sufficiently tightened, increasing injury risk in a collision.

    Product
    HYUNDAI — HYUNDAI SANTA FE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·059-2017·2017-06-05

    Creation Gardens Recalls Raw Beef Products Due to E. coli O157:H7

    Creation Gardens is recalling approximately 22,832 pounds of raw ground beef and primal cuts shipped to food service locations in four states due to possible E. coli O157:H7 contamination.

    Product
    Creation Gardens — Creation Gardens Inc. Recalls Ground Beef and Beef Primal Cut Products Due to Possible E. coli O157:H7 Contamination
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·17V362000·2017-06-02

    Thor Motor Coach Recalls 2017 Challenger 37YT Motorhomes for Exhaust Defect

    Thor Motor Coach is recalling 2017 Challenger 37YT motorhomes because the generator exhaust pipe may be mislocated or missing, creating a carbon monoxide risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·058-2017·2017-06-02

    P&S Bakery Recalls Pepperoni Rolls Due to Foreign Matter Contamination

    P&S Bakery is recalling approximately 2,959 pounds of Gia Russa brand pepperoni rolls due to possible contamination with clear meat casing. No illnesses have been reported.

    Product
    P&S Bakery, Inc — P&S Bakery, Inc. Recalls Pepperoni Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·17V360000·2017-06-02

    MCI Recalls 2014-2017 J4500 Motor Coaches Due to Brake Hose Defect

    Motor Coach Industries is recalling 2014-2017 J4500 motor coaches because over-tightened front brake hose clamps may damage the hoses, potentially increasing stopping distance and crash risk.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V355000·2017-06-01

    Mazda Recalls 2004 RX-8 Vehicles for Front Suspension Control Arm Defect

    Mazda is recalling 2004 RX-8 vehicles because a crack in the front suspension lower control arm ball joint socket may cause the ball joint to separate, potentially leading to loss of steering control.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V357000·2017-06-01

    Polaris Recalls 2015-2017 Slingshot Vehicles for Missing Swingarm Grommets

    Polaris is recalling 2015-2017 Slingshot vehicles because missing grommets on replacement swingarms may allow debris to contaminate the rear wheel speed sensor, disabling ABS and traction control.

    Product
    POLARIS — POLARIS SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2246-2017·2017-05-31

    Chef Luca's Frozen Lasagna Recalled for Undeclared Eggs

    Italian Gluten Free Foods CL is recalling Chef Luca's Lasagna Al Forno due to undeclared eggs. The product was distributed in nine states.

    Product
    Chef Luca's Italian Gluten Free Foods Lasagna Al Forno Baked Cheese Lasagna, 15 oz . frozen UPC Code: 85573103116
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Drugs)·D-0864-2017·2017-05-31

    Hyland's Baby Nighttime Teething Tablets Recalled for Inconsistent Belladonna Alkaloids

    Standard Homeopathic Company is recalling Hyland's Baby Nighttime Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids.

    Product
    Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated), Calcarea Phosphorica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Magnesia Phosphorica 6X HPUS, Rheum 6X HPUS, Silicea 12X HPUS] Quick-Dissolving Tablets, 135-count…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2266-2017·2017-05-31

    Huson Valley Farms Recalls Cashew Butter for Listeria Contamination

    Huson Valley Farms is recalling 5,022 jars of Nutty INFUSIONS Roasted Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.

    Product
    Nutty INFUSIONS Roasted Cashew Butter, NET WT. 10 OZ (284 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2241-2017·2017-05-31

    Starbucks Slow Roasted Ham & Swiss Sandwich Recalled for Listeria

    SK Food Group is recalling Starbucks Slow Roasted Ham & Swiss Breakfast Sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Slow Roasted Ham & Swiss Breakfast Sandwich, Fully Cooked/Keep Frozen/Perishable Net Wt 5.6 oz (159 g) MANUFACTURED EXCLUSIVELY FOR STARBUCKS COFFEE COMPANY SEATTLE, WA 98134 UPC 7 62111 10495 1
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-2245-2017·2017-05-31

    Phoenix Food Recalls Dip Trio Mix for Possible Salmonella Contamination

    Phoenix Food, LLC is recalling 11,936 boxes of Dip Trio Mix due to possible Salmonella contamination. The product was distributed across 25 U.S. states and Canada.

    Product
    Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103 www.homemadegourmet.com
    Category
    Food
    Distribution
    24 states
  • CriticalFDA (Drugs)·D-0863-2017·2017-05-31

    Hyland's Baby Teething Tablets Recalled for Inconsistent Belladonna Alkaloid Levels

    Standard Homeopathic Company is recalling Hyland's Baby Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from label claims.

    Product
    Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS, Chamomilla 6X HPUS, Coffea Cruda 6X HPUS, Belladonna 12X HPUS (0.0000000000003% alkaloids, calculated)] Quick-Dissolving Tablets, packaged in a) 40-count bottles (NDC 54973-3127-3) (UPC 3 54973 31273 9); b) 135-count…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0867-2017·2017-05-31

    Envy Me Recalls LaBri's Body Health Atomic Due to Undeclared Sibutramine

    Envy Me is recalling LaBri's Body Health Atomic capsules because the product contains undeclared Sibutramine and was marketed without an approved NDA/ANDA.

    Product
    LaBri's Body Health Atomic, 60 capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2269-2017·2017-05-31

    Nutty INFUSIONS Ginger Wasabi Cashew Butter Recalled for Listeria Contamination

    Huson Valley Farms is recalling Nutty INFUSIONS Ginger Wasabi Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.

    Product
    Nutty INFUSIONS Ginger Wasabi Cashew Butter, NET WT. 10 OZ (284 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0862-2017·2017-05-31

    Hospira Recalls Dextrose Injection Syringes Due to Human Hair Particulate

    Hospira is recalling 71,550 syringes of Infant 25% Dextrose Injection because human hair was found in an internal sample. The product was distributed nationwide and in Puerto Rico.

    Product
    DEXTROSE — DEXTROSE (DEXTROSE MONOHYDRATE)
    Category
    Drug
    Distribution
    Distributed nationwide