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 deaths or serious injuries are reported, 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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Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

1176–1200 of 26155

  • HighFDA (Food)·H-0650-2026·2026-04-15

    Zarlengo's Chocolate Chocolate Chip Gelato Recalled for Undeclared Soy Allergen

    Zarlengo Italian Ice is recalling Chocolate Chocolate Chip Gelato in multiple sizes because soy lecithin is listed in the ingredients but soy is not declared in the allergen statement, posing a risk to consumers with soy allergies.

    Product
    Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminat
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·H-0663-2026·2026-04-15

    Vital Nutrients Aller-C supplement recalled for undeclared allergens

    Blueroot Health, Inc. is recalling Vital Nutrients Aller-C vitamin supplements because they contain undeclared egg, soy, and hazelnut allergens, posing a risk to consumers with allergies to these ingredients.

    Product
    Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count bottles
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0651-2026·2026-04-15

    Zarlengo's Chocolate Gelato recalled for undeclared soy allergen

    Zarlengo's Chocolate Gelato is recalled because soy lecithin is in the product but soy is not listed in the allergen contains statement. The mislabeling affects people with soy allergies.

    Product
    Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0445-2026·2026-04-15

    Isotretinoin 30 mg capsules recalled due to potency variation

    Teva Pharmaceuticals is recalling Isotretinoin 30 mg capsules with potency defects. Affected lots contain capsules that are either superpotent or subpotent from normal specifications.

    Product
    ISOTRETINOIN — ISOTRETINOIN (ISOTRETINOIN)
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-1787-2026·2026-04-15

    Cook Medical NCompass Nitinol Stone Extractor: Incorrect Expiration Dating

    Cook Medical is recalling certain NCompass Nitinol Stone Extractor units with expiration dates exceeding true shelf life. Affected healthcare providers should discontinue use and contact the manufacturer.

    Product
    COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.4-115-NC3, Order Number G36250; Reference Part Number C-NTSE-2.4-115-NCT4, Order Number G36251.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1792-2026·2026-04-15

    COOK MEDICAL Wayne Pneumothorax Tray: Incorrect Expiration Date Labeling

    Cook Medical issued a Class II recall of 318 Wayne Pneumothorax Trays distributed worldwide because the devices were labeled with expiration dates exceeding their true shelf life.

    Product
    COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537; Reference Par
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1794-2026·2026-04-15

    MicroScan Diagnostic Device Recalled for Manufacturing Defect in Antimicrobial Susceptibility Test

    Beckman Coulter is recalling MicroScan Neg Multidrug Resistant test kits due to incorrect manufacturing processing of the in vitro antimicrobial test. The defect may affect diagnostic accuracy.

    Product
    MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Intended Use- For use with MicroScan Dried Gram Negative MIC/Combo Panels and Dried Gram Negative Breakpoint Combo Panels. MicroScan panels are designed for use in determining antimicrobial agen
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0424-2026·2026-04-15

    Sodium Chloride Injection Batch Recalled Due to Sterility Assurance

    Fresenius Kabi USA, LLC is recalling batch 6402413 of 0.45% Sodium Chloride Injection, USP, due to lack of assurance of sterility. The affected batch was distributed nationwide, including Alaska and Puerto Rico.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0426-2026·2026-04-15

    Sodium Chloride Injection Batches Recalled for Lack of Sterility Assurance

    Fresenius Kabi USA, LLC is recalling sodium chloride 0.9% intravenous injections because the manufacturer cannot assure sterility. Affected batches were distributed nationwide and in Puerto Rico and Alaska.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1777-2026·2026-04-15

    Cook Medical Micro Wire Guide: Mislabeled Expiration Dates Exceed True Shelf Life

    Cook Medical is recalling the Approach CTO-18 Micro Wire Guide due to mislabeled expiration dates that exceed the product's actual shelf life. The recall affects 75 units distributed worldwide.

    Product
    COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0427-2026·2026-04-15

    Sodium Chloride Injection Recalled for Lack of Sterility Assurance

    Fresenius Kabi is recalling specific batches of 0.9% Sodium Chloride Injection due to lack of sterility assurance. The affected intravenous medication was distributed nationwide, including Alaska and Puerto Rico.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0441-2026·2026-04-15

    Vancomycin HCI Injection Recalled for Sterility and Port Detachment Issues

    Fagron Compounding Services is recalling Vancomycin HCI injections nationwide due to lack of sterility assurance and potential detachment of a break-off-part from the administration port. Affected healthcare facilities should refer to FDA guidance.

    Product
    Vancomycin HCI, 1.5 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5085-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0440-2026·2026-04-15

    Vancomycin Injectable Solution Recalled for Sterility and Mechanical Defects

    The FDA is recalling Vancomycin HCI injectable solution (34,260 bags) distributed nationwide due to lack of sterility assurance and risk of a blue break-off-part detaching from the administration port.

    Product
    Vancomycin HCI, 1.25 grams added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5083-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0428-2026·2026-04-15

    Sodium Chloride Injection Recalled for Lack of Sterility Assurance

    Fresenius Kabi recalled specific batches of 0.9% sodium chloride injection because sterility cannot be assured. The affected batches were distributed throughout the United States, Alaska, and Puerto Rico.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0438-2026·2026-04-15

    Norepinephrine Injection Recalled for Sterility Assurance and Component Defect

    Fagron Compounding Services is recalling norepinephrine bitartrate injection nationwide due to lack of sterility assurance and a blue break-off part that could detach from the administration port.

    Product
    norepinephrine Bitartrate,16mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5026-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0439-2026·2026-04-15

    Norepinephrine Injectable Recalled Due to Sterility and Equipment Safety Concerns

    Fagron Compounding Services is recalling 5,140 bags of norepinephrine injectable nationwide due to lack of sterility assurance and a potentially detachable component in the administration port. The affected lots expire between April and July 2026.

    Product
    norepinephrine Bitartrate, 32mg per 250mL 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5027-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0434-2026·2026-04-15

    Intravenous Sodium Chloride Injection Recalled Due to Sterility Assurance Failure

    Fresenius Kabi USA is recalling a batch of 0.9% Sodium Chloride Injection due to lack of assurance of sterility. The product was distributed nationwide, in Alaska, and Puerto Rico.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0442-2026·2026-04-15

    Injectable vancomycin drug recalled for sterility assurance and port defects

    Fagron Compounding Services is recalling Vancomycin HCL injectable solutions due to lack of sterility assurance and risk that a blue break-off part could detach from the administration port.

    Product
    Vancomycin HCL, 1 gram added to 250 mL, 0.9% Sodium Chloride Injection USP, Fagron Sterile Services, 8710 34th St. N. Wichita, KS 67226, NDC 71266-5082-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1789-2026·2026-04-15

    COOK Spectrum Central Venous Trays recalled for overstated expiration dates

    Cook Incorporated is recalling certain COOK Spectrum Central Venous Trays that are labeled with expiration dates exceeding their actual shelf life, creating risks of compromised sterility and device degradation.

    Product
    COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-RD, Order Number G44800; Reference Part Number C-UTLMYJ-701J-ABRM-HC-IHI-FST-A-RD, Order Number G44809; Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-FST-A-RD, Order Number G
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1772-2026·2026-04-15

    MicroScan Neg MIC 3J Diagnostic Panels Recalled for Manufacturing Defects

    Beckman Coulter is recalling MicroScan Neg MIC 3J diagnostic panels due to manufacturing errors affecting test accuracy. One well per panel is missing a required drug while others contain double the intended amount of antibiotics.

    Product
    MicroScan Neg MIC 3J REF C54814
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1769-2026·2026-04-15

    Tornier HRS Max Shoulder Implant Parts Mislabeled With Wrong System Compatibility

    Tornier HRS Max orthopedic implant parts were mislabeled as compatible with the HRS Max system, but are actually compatible only with the older HRS system and will not work with HRS Max components.

    Product
    Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102 3. TORNIER HRS Max Trial, Cat. No. ARS10252
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1653-2026·2026-04-15

    ARTIS Pheno and Icono X-Ray Systems Recalled for Inaccurate Dose Display

    ARTIS pheno and ARTIS Icono X-ray systems may display dramatically higher radiation dose readings than actually applied during patient examinations. The actual dose remains compliant with regulations, though the display error could lead clinicians to question equipment accuracy.

    Product
    ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1779-2026·2026-04-15

    Cook Medical Tracheostomy Introducer Sets Labeled with Incorrect Expiration Dates

    Cook Medical has recalled 916 units of Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets worldwide because the labels show expiration dates that exceed the true shelf life of the devices.

    Product
    COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Reference Part Number C-PTIS-100-HC-G-EU, Order Number G57685; Reference Part Number C-PTIS-100-HC-G-NA, Order Number G57682; Reference Part Number C-PTIS-100-UNL-HC-G-EU, Order Number G57687; Refer
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1793-2026·2026-04-15

    Multi-parameter Command Module Cardiac Output Measurement May Be Inaccurate

    Spacelabs Multi-parameter Command Module Model 91496 may provide inaccurate cardiac measurements in Auto mode due to a circuit board defect, potentially delaying diagnosis and increasing risk of fluid overload.

    Product
    Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor
    Category
    Medical Device
    Distribution
    Distributed nationwide