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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

34851–34875 of 39756

  • SevereFDA (Drugs)·D-374-2013·2013-05-22

    Green Valley Drugs Recalls Hydroxocobalamin Injection Due to Sterility Concerns

    Green Valley Drugs is recalling 135 vials of Hydroxocobalamin Injection nationwide due to a lack of assurance of sterility in its compounding and quality control processes.

    Product
    Hydroxocobalamin Injection, all strengths and all presentations including a) Hydroxocobalamin 1000 mcg/mL 30mL and b) Hydroxocobalamin 1000 mcg/mL 10 mL P.F., Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-375-2013·2013-05-22

    Green Valley Drugs Recalls Hydroxyprogesterone Caproate Injection Due to Sterility Concerns

    FVS Holdings, Inc. dba. Green Valley Drugs is recalling 229 vials of Hydroxyprogesterone Caproate Injection nationwide due to lack of assurance of sterility.

    Product
    Hydroxyprogesterone Caproate Injection, all strengths and all presentations including Hydroxyprogesterone Caproate 250 mg/mL 1 mL, 4 mL, 5 mL, 10 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-365-2013·2013-05-22

    Green Valley Drugs Recalls Estradiol Valerate Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Estradiol Valerate Injection vials because the pharmacy could not ensure the products were sterile. This affects 243 vials distributed nationwide.

    Product
    Estradiol Valerate Injection, all strengths and all presentations including a) Estradiol Valerate 40-10 mL and b) Estradiol Valerate 40-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1342-2013·2013-05-22

    Centerville Pie Company Recalls Clam Pies Due to Undeclared Anchovies

    Centerville Pie Company is recalling 52 clam pies sold in Massachusetts because they contain undeclared anchovies, a potential allergen risk.

    Product
    Centerville Pie Company Clam Pie, 2 lb (Large) and 1 lb (Small)
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1408-2013·2013-05-22

    Lisy Corp. Recalls Sazonador de Carnes Meat Seasoning for Undeclared Soy

    Lisy Corp. is recalling Sazonador de Carnes meat seasoning in 5 oz, 14 oz, and 28 oz sizes due to undeclared soy. The product was distributed in 12 states.

    Product
    Sazonador de Carnes (Meat Seasoning) in 5 oz, 14 oz, and 28 oz
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Drugs)·D-340-2013·2013-05-22

    Green Valley Drugs Recalls Alpha Lipoic Acid Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Alpha Lipoic Acid Injection vials because the pharmacy could not ensure the products were sterile.

    Product
    Alpha Lipoic Acid Injection, all strengths and all presentations including 25 mg/mL, 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-341-2013·2013-05-22

    Green Valley Drugs Recalls Amikacin Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Amikacin Injection because the pharmacy could not ensure the sterility of the compounded products. The recall covers all strengths and presentations of the drug.

    Product
    Amikacin Injection, all strengths and all presentations including 50, 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-390-2013·2013-05-22

    Green Valley Drugs Recalls Methylprednisolone and Bupivacaine Injection Due to Sterility Concerns

    FVS Holdings, Inc. dba. Green Valley Drugs is recalling Methylprednisolone and Bupivacaine Injection due to a lack of assurance of sterility and quality control concerns.

    Product
    Methylprednisolone and Bupivacaine Injection, all strengths and all presentations including Methylpred80mg/bupivacaine0.25% syr; Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-376-2013·2013-05-22

    Green Valley Drugs Recalls Ketorolac Injection Due to Sterility Concerns

    Green Valley Drugs is recalling 3,289 vials of Ketorolac Injection nationwide due to a lack of assurance of sterility in its compounding and quality control processes.

    Product
    Ketorolac Injection, all strengths and all presentations including a) Ketorolac 30 mg/mL 10 mL MDV, b) Ketorolac 30 mg/mL 2 mL SDV, c) Ketorolac 30 mg/mL 1 mL SDV, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-406-2013·2013-05-22

    Green Valley Drugs Recalls Nandrolone and Testosterone Injections for Sterility Concerns

    Green Valley Drugs is recalling Nandrolone Decanoate and Testosterone Cypionate injections due to a lack of assurance of sterility and quality control concerns.

    Product
    Nandrolone Decanoate and Testosterone Cypionate Injection, all strengths and all presentations including a) Nandrolone 100 mg/mL TestCyp 100 mg/mL 10 mL and b) Nandrolone 100 mg/mL TestCyp 200 mg/mL 10 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1409-2013·2013-05-22

    Lisy Corp. Recalls Sazon Perfecta Seasoning Due to Undeclared Soy

    Lisy Corp. is recalling Sazon Perfecta seasoning in 4 oz, 12 oz, and 24 oz packages because it contains undeclared soy.

    Product
    Sazon Perfecta (Perfect Seasoning) in 4 oz, 12 oz, and 24 oz
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Drugs)·D-412-2013·2013-05-22

    Green Valley Drugs Recalls Sterile Testosterone and Nandrolone Injections

    Green Valley Drugs is recalling specific lots of sterile hormone injections due to a lack of assurance of sterility and quality control concerns.

    Product
    Testosterone Propionate, Testosterone Cypionate, and Nandrolone Decanoate Injection, all strengths and all presentations including Test Prop 100 mg/Test Cyp 50 mg/nandro dec 150 mg/ml, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-323-2013·2013-05-22

    Super Power capsules recalled for containing unapproved sildenafil

    D& S Herbals, LLC is recalling Super Power capsules because they contain sildenafil, an unapproved drug ingredient.

    Product
    Super Power capsules, Proprietary Blend 570 mg, packaged in 2-count capsules per blister pack, Distributed by: Freedom Trading, NJ 08863, UPC 7 18122 90678 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-399-2013·2013-05-22

    Green Valley Drugs Recalls Phosphatidylcholine Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Phosphatidylcholine and Sodium Deoxycholate Injection due to a lack of assurance of sterility in compounded products.

    Product
    Phosphatidylcholine and Sodium Deoxycholate Injection, all strengths and all presentations including Phospha_Deoxy-35-30-50 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1383-2013·2013-05-22

    Carson's Assorted Cookie Pack Recalled for Undeclared Allergens

    Carson's Country Market is recalling Assorted Cookie Packs sold in New York due to undeclared walnuts, wheat, milk, and peanut butter.

    Product
    CARSON'S HOMEMADE PIES AND OTHER GOOD THINGS brand ASSORTED COOKIE PACK Chocolate Chip - Fudge Brownie - Vanilla Drop - Molasses - Oatmeal Raisin - Peanut Butter - Pumpkin, NET WT. 14 OZ., UPC 7 53182 15240 0 --- Sanborn, NY 14132 --- The cookies are packaged in clear, hard…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-388-2013·2013-05-22

    Green Valley Drugs Recalls Methylprednisolone and Marcaine Injections for Sterility Concerns

    FVS Holdings, Inc. dba. Green Valley Drugs is recalling 607 vials of Methylprednisolone Acetate and Marcaine Injection due to lack of assurance of sterility and quality control concerns.

    Product
    Methylprednisolone Acetate and Marcaine Injection, all strengths and all presentations including a) Methylpred 80 mg/mL and Marcaine 0.25%-2.75, b) Methylpred_Marc-0.25-0.27, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-411-2013·2013-05-22

    Green Valley Drugs Recalls Taurine Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Taurine Injection products because the compounding pharmacy lacked assurance of sterility and had quality control concerns.

    Product
    Taurine Injection, all strengths and all presentations including a) Taurine 50 mg/mL, b) Taurine-50-30 mL, c) Taurine-50 mg-30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1386-2013·2013-05-22

    Heartland Gourmet Gluten Free Pizza Crust Mix Recalled for Milk Mislabeling

    Heartland Gourmet is recalling gluten-free pizza crust mix labeled as dairy-free but containing milk. The recall affects 204 boxes distributed to schools, online, and retail in TX, MN, CO, and Canada.

    Product
    Heartland Gourmet Gluten Free rosemary basil pizza crust mix, DAIRY FREE, packaged in 15.4-oz. boxes. Manufactured by: Heartland Gourmet, LLC, Lincoln, NE.
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-398-2013·2013-05-22

    Green Valley Drugs Recalls Phenylephrine Injection Due to Sterility Concerns

    Green Valley Drugs is recalling Phenylephrine Injection vials because the pharmacy could not ensure the products were sterile.

    Product
    Phenylephrine Injection, all strengths and all presentations including Phenylephrine 1% 30 mL, Rx only, Green Valley Drugs, 1850 Whitney Mesa, #180, Henderson, NV 89014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V209000·2013-05-17

    Elite Recalls 2012 Livestock Trailers Due to Brake Actuator Wear

    Elite Trailer Manufacturing is recalling 2012 Livestock Gooseneck trailers because a manufacturing defect in the hydraulic brake actuator could cause a loss of braking ability.

    Product
    ELITE — ELITE LIVESTOCK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V214000·2013-05-17

    Pierce Emergency Vehicles Recalled for Door Handle Spring Defect

    Pierce is recalling 2007-2013 Velocity, Impel, and Dash CF emergency vehicles because door handle springs may be too weak to prevent doors from opening in a crash.

    Product
    PIERCE — PIERCE VELOCITY, IMPEL, DASH CF
    Category
    Vehicle
    Distribution
    Distributed nationwide