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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30126–30150 of 39756

  • SevereFDA (Devices)·Z-0085-2015·2014-11-12

    Baxter INTRA VIA Container Recalled for Particulate Matter in Fluid Path

    Baxter Healthcare is recalling 20,448 units of INTRA VIA containers due to particulate matter found inside the fluid path.

    Product
    Baxter 2B8013 Empty INTRA VIA Container with PVC Ports (Sterile, nonpyrogenic fluid path) ,500 ml. Admixture Products and Accessories The lntraVia Empty Plastic Container is intended for use in the preparation and administration of drug admixtures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0227-2015·2014-11-12

    Vancomycin Injectable Syringes Recalled for Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Vancomycin injectable syringes due to quality control issues affecting sterility assurance identified during an FDA inspection.

    Product
    VANCOMYCIN, 1mg/0.1mL, injectable, 0.2 mL plastic syringe, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0168-2015·2014-11-12

    IBA Dosimetry Recalls COMPASS Software Due to Dose Calculation Errors

    Iba Dosimetry Gmbh is recalling COMPASS software version 3.1 because a defect may prevent detection of dose distribution errors, potentially leading to incorrect radiation doses during treatment.

    Product
    COMPASS, Model No. SW Version 3.1, catalogue number CS10-100 (medical Linear accelerator) radiological
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0186-2015·2014-11-12

    FDA Recalls Dexpantenol Injectable Due to Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Dexpantenol injectable vials due to quality control issues affecting sterility assurance identified during an FDA inspection.

    Product
    DEXPANTHENOL with preservative, 250 mg/mL, injectable, 30 mL glass vial, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0224-2015·2014-11-12

    Testosterone Cypionate Injectable Recalled for Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Testosterone Cypionate injectable vials due to quality control issues affecting sterility assurance identified during an FDA inspection.

    Product
    TESTOSTERONE CYPIONATE (SESAME OIL/CMPD), 200mg/mL, injectable, 5 mL glass vial, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0219-2015·2014-11-12

    FDA Recalls Prednisolone Sodium Phosphate Eye Drops for Sterility Concerns

    Oregon Compounding Centers is recalling Prednisolone Sodium Phosphate ophthalmic drops due to quality control issues affecting sterility assurance.

    Product
    PREDNISOLONE Sodium Phosphate, 1%, Ophthalmic, 1 mL plastic dropper bottle, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0213-2015·2014-11-12

    FDA Recalls Papaverine Injection Due to Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Papaverine HCL/Phentolamine Mes/Prostaglandin injections due to quality control issues affecting sterility assurance.

    Product
    PAPAVERINE HCL/PHENTOLAMINE MES/PROSTAGLANDIN, 23mg/0. 96mg/19.23mcg, injectable, 1.7 mL glass vial, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0191-2015·2014-11-12

    Ganciclovir Syringes Recalled for Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Ganciclovir syringes due to quality control issues affecting sterility assurance identified during an FDA inspection.

    Product
    GANCICLOVIR, preservative free, 0.2mg/0.05mL, injectable, 0.1 mL plastic syringe, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0176-2015·2014-11-12

    FDA Recalls Injectable Ascorbic Acid Vials Due to Sterility Concerns

    Oregon Compounding Centers is recalling injectable ascorbic acid vials because quality control issues observed during an FDA inspection present a potential risk to sterility assurance.

    Product
    ASCORBIC ACID (with Preservative), 500 mg/mL, injectable, 100 mL glass vial, RX, Creative Compounds, Wilsonville, OR 97070.
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0222-2015·2014-11-12

    Sodium Chloride Inhalation Solution Recalled for Sterility Assurance Concerns

    Oregon Compounding Centers is recalling Sodium Chloride Inhalation 7% solution due to quality control issues affecting sterility assurance.

    Product
    SODIUM CHLORIDE INHALATION, 7%, Solution for inhalation, 3 mL plastic vial, RX, Creative Compounds, Wilsonville, OR 97070
    Category
    Drug
    Distribution
    2 states
  • SevereNHTSA·14V722000·2014-11-10

    Kenworth Heavy Trucks Recalled for Undersized Wire Gauge Fire Risk

    PACCAR is recalling 2015 Kenworth heavy trucks because an undersized wire in the instrument panel harness may overheat, increasing the risk of a vehicle fire.

    Product
    KENWORTH — KENWORTH T660, T800, W900, C500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V717000·2014-11-10

    Daimler Recalls 2014-2015 Freightliner Trucks Due to Brake Valve Defect

    Daimler is recalling 2014-2015 Freightliner trucks because defective air brake valves may reduce braking performance and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER 122SD, ARGOSY, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V719000·2014-11-10

    GM Recalls 2015 Trucks and SUVs for Power Steering Loss

    General Motors is recalling 2015 Chevrolet and GMC vehicles because a steering module defect may cause sudden loss of power assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC SUBURBAN, YUKON, TAHOE, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V712000·2014-11-07

    Forest River Recalls 2015 Wildwood and Salem Trailers for Draw Bar Defect

    Forest River is recalling 2015 Wildwood and Salem Ice Cabin trailers because the draw bar may break, potentially causing the trailer to detach from the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V716000·2014-11-07

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Brake Valve Defect

    PACCAR is recalling specific 2014-2015 Kenworth and Peterbilt trucks because defective parking brake valves may reduce braking performance and increase crash risk.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, 220, MODEL 220, K370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·076-2014·2014-11-06

    CS Best Food Recalls Pork Sausage Links Due To Undeclared Allergens

    CS Best Food Inc. is recalling pork sausage links containing undeclared wheat and soy allergens. The products were distributed in California and Washington.

    Product
    CS Best Food, Inc. — California Firm Recalls Pork Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-0082-2015·2014-11-05

    Herb Garden Productions Recalls WildForce Green Formula Due to Salmonella Risk

    Herb Garden Productions is recalling WildForce Green Formula because Nettle Leaf Powder may contain Salmonella.

    Product
    WildForce Green Formula, The Power of Wild Plants, 430 grams. bottles in 2500cc food grade white plastic bottle. Manufacturer: Herbally Grounded LLC., Curtiss Harris 7023640090 3744 W. Meade Ave. Ste. 11a Las Vegas, NV 89102
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0083-2015·2014-11-05

    WildForce Super Plant Protein Recalled for Potential Salmonella Contamination

    Herb Garden Productions is recalling WildForce Super Plant Protein because Nettle Leaf Powder may contain Salmonella.

    Product
    WildForce Super Plant Protein, 2 lbs (32 oz) Bottled in 2500cc food grade white plastic bottle. Manufacturer: Herbally Grounded LLC., Curtiss Harris 7023640090 3744 W. Meade Ave. Ste. 11a Las Vegas, NV 89102
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0081-2015·2014-11-05

    Herbally Grounded Hello Blossom Capsules Recalled for Salmonella Risk

    Herb Garden Productions is recalling Herbally Grounded Hello Blossom capsules because the nettle leaf powder ingredient may contain Salmonella.

    Product
    Herbally Grounded Hello Blossom 120 ct Vegetarian Capsule Formula, bottle in 20cc food grade amber glass bottle. Manufacturer: Herbally Grounded LLC., Curtiss Harris 7023640090 3744 W. Meade Ave. Ste. 11a Las Vegas, NV 89102
    Category
    Food
    Distribution
    0 states
  • CriticalFDA (Food)·F-0084-2015·2014-11-05

    Jinga Panfried Anchovy Recall for Listeria Contamination

    Jinga brand Panfried Anchovies are being recalled due to Listeria monocytogenes contamination found by Virginia state officials.

    Product
    JINGA brand PANFRIED ANCHOVY(S), NET WT. 2 oz. and 4 oz., KEEP REFRIGERATED -- JINGA 44-28 55TH AVE., MASPETH, NY 11378 --- The product is packaged in clear, hard plastic containers.
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0230-2015·2014-11-05

    FDA Recalls Calcium Glucosate Injection Due to Microbial Contamination

    Specialty Compounding, LLC is recalling Calcium Gluconate 2 gm in 100 mL Sodium Chloride 0.9% for Injection due to non-sterility and microbial contamination.

    Product
    CALCIUM GLUCONATE 2 gm (PF) PRESERVATIVE FREE in 100 mL Sodium Chloride 0.9% for Injection, Rx Only Manufactured by Specialty Compounding, 211 S. Bell Blvd, Cedar Park, TX 78613
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0071-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Cromolyn Sodium Inhalant Solution

    Martin Avenue Pharmacy is voluntarily recalling Cromolyn sodium 1% inhalant solution due to sterility assurance concerns identified during an FDA inspection.

    Product
    Cromolyn sodium 1% inhalant solution packaged in a 3 mL or 7 mL vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0085-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including Hyaluronidase base vehicle, due to quality control issues affecting sterility assurance.

    Product
    Hyaluronidase base vehicle (PF) solution packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0111-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including PGE 1, due to quality control observations that risk sterility assurance.

    Product
    PGE 1, 40 mcg/mL injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide