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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9301–9325 of 113902

  • HighFDA (Devices)·Z-1752-2025·2025-05-21

    Pruitt Irrigation Occlusion Catheter Recalled for Incomplete Sterile Seals

    LeMaitre Vascular is recalling Pruitt Irrigation Occlusion Catheters (Catalog Numbers 2102-09, E2102-09) due to incomplete sterile barrier seals found during internal testing. The defect affects approximately 26,872 units distributed nationwide and internationally.

    Product
    Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2025·2025-05-21

    Philips Intera 1.5T MRI Quadrature Body Coil seal adhesive failure

    Philips is recalling Intera 1.5T MRI systems due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and contact patient skin during scanning.

    Product
    Intera 1.5T, Model Numbers: 781195 and 781295;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0801-2025·2025-05-21

    New England Village Snacks Mix Recalled for Undeclared Allergens

    New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.) is being recalled due to undeclared almonds and sesame. Consumers with allergies to these ingredients should not consume the product.

    Product
    New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1766-2025·2025-05-21

    Centurion Sterile Weitlaner Retractor recalled for sterile packaging puncture risk

    Medline Industries is recalling Centurion Sterile Weitlaner Retractor 3 x 4 Prong units because the retractors may puncture through the sterile packaging. The product is distributed nationwide.

    Product
    Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0790-2025·2025-05-21

    Vanilla Frozen Yogurt Recalled for Possible Plastic Foreign Material

    Wells Enterprises is recalling Vanilla Frozen Yogurt 3-gallon tubs due to the possible presence of plastic material in the product.

    Product
    Vanilla Frozen Yogurt, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 00070640022144, Item: 1352604
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0786-2025·2025-05-21

    Quick Blend Vanilla Flavored Ice Cream recalled for plastic contamination

    Wells Enterprises is recalling Quick Blend Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.

    Product
    Quick Blend Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050604, Item: 773034
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0804-2025·2025-05-21

    Blueberry Lemon Scones recalled for undeclared soy allergen

    The Hot Chocolatier - St. Elmo, LLC is recalling Blueberry Lemon Scones sold in bulk bakery boxes because they contain undeclared soy, a common allergen.

    Product
    Blueberry Lemon Scones, bulk packaged in bakery boxes. Products are sold at retail in pastry cases and not individually labeled.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1776-2025·2025-05-21

    Philips Intera 1.5T MRI Scanner Body Coil Seal Failure Recall

    Philips is recalling 103 Intera 1.5T MRI scanners worldwide because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could cause skin abrasions, bruises, lacerations, hair loss, or tissue injury to patients.

    Product
    Intera 1.5T Master/Nova, Model Number: 781106;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0783-2025·2025-05-21

    Scooper Hero Ice Cream recalled for possible plastic contamination

    Wells Enterprises is recalling Scooper Hero Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.

    Product
    Scooper Hero Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050642, Item: 487054
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1770-2025·2025-05-21

    Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal

    Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.

    Product
    Enterprise 1.5T, Model Number: 781145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0784-2025·2025-05-21

    Cotton Candy Flavored Ice Cream recalled for possible plastic contamination

    Wells Enterprises is recalling Cotton Candy Flavored Ice Cream 3-gallon tubs because foreign plastic material may be present in the product.

    Product
    Cotton Candy Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050482, Item: 662429
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0782-2025·2025-05-21

    Country Rich Vanilla Ice Cream recalled for possible plastic contamination

    Wells Enterprises is recalling Country Rich Vanilla Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.

    Product
    Country Rich Vanilla Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640600052, Item: 102010
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0417-2025·2025-05-21

    La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene Contamination

    La Roche-Posay Effaclar Duo acne treatment is being recalled due to detected trace levels of benzene. The recall affects 2,226,801 units distributed nationwide.

    Product
    La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, 40 mL (135 FL. OZ.) Tube per carton, La Roche-Posay LLC, 10 Hudson Yards, New York, NY 10001, La Roche-Posay, Laboratoire Dermatologique, CAI 86270, La Roche-
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0418-2025·2025-05-21

    La Roche-Posay Effaclar Acne Treatment Kits Recalled Nationwide

    L'Oreal USA is recalling La Roche-Posay Effaclar 3-Step Acne Routine Kits nationwide due to trace levels of benzene detected in one lot. As a precaution, all Effaclar Duo Dual Action Acne Treatment lots are included in the recall.

    Product
    La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne System, 3 Step Acne Routine Kit, Medicated Gel Cleanser 3.4 fl. oz. (100 mL) Tube, Clarifying Solution 3.4 fl. oz. (100 mL) Tube, Dual Action Acne Treatment 0.7 fl. oz. (20 mL: UPC 883140035275) Tube, (benzoyl
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0793-2025·2025-05-21

    Gordon Choice Vanilla Flavored Ice Cream Recall for Plastic Contamination

    Gordon Choice Vanilla Flavored Ice Cream in 3-gallon tubs is being recalled because plastic material may be present in the product. The affected ice cream was distributed to 103 distribution centers across the US.

    Product
    Gordon Choice Vanilla Flavored Ice Cream, 3 GAL, FOR DISTRIBUTION EXCLUSIVELY BY GORDON FOOD SERVICE, WYOMING, MI 49509, UPC: 00093901820730, Item: 1367499
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1765-2025·2025-05-21

    Centurion Sterile Weitlaner Retractor recalled for packaging puncture risk

    Medline Industries is recalling Centurion Sterile Weitlaner Retractors (2,100 units) due to potential puncture damage to sterile packaging. The defect could compromise the sterility of the surgical instrument.

    Product
    Centurion Sterile Weitlaner Retractor, Reorder: 67315
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0419-2025·2025-05-21

    La Roche-Posay Effaclar Duo Acne Treatment Recalled for Benzene

    L'Oreal USA is voluntarily recalling all lots of La Roche-Posay Effaclar Duo Dual Action Acne Treatment due to detected trace levels of benzene in a specific lot.

    Product
    La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne Treatment, 5.5% Benzoyl Peroxide Acne Medication, a) UPC 3606000508804, 20 mL (0.7 fl. oz.) Tube per Carton, b) 883140500759, 40 mL (1.35 fl. oz.) Tube per Carton, La Roche-Posay LLC, 10 Hudson Yards, New Yor
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1745-2025·2025-05-21

    Contour Gold Eyelid Weight implants recalled for mislabeling

    Meddev Corp is recalling Contour Gold Eyelid Weight implants (Model LL3012) due to mislabeling. Thirty-four weights distributed nationwide are affected.

    Product
    Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid Weight, 1.2 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the gravity-assisted treatment of protracted permanent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1741-2025·2025-05-21

    Halyard CHRIST SUTURE KIT surgical needles coating defect recall

    AVID Medical is recalling Halyard CHRIST SUTURE KIT units due to a raw material issue in the needle coating that may cause silicone to be removed during use, potentially affecting surgical performance.

    Product
    Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1747-2025·2025-05-21

    FoundationOne Companion Diagnostic reports clinically relevant variants requiring amendment

    Foundation Medicine is recalling four FoundationOne Companion Diagnostic (F1CDx) test reports sent to customers that contained clinically relevant variants requiring amendment, including one with an incorrect negative companion diagnostic claim.

    Product
    FoundationOne Companion Diagnostic (F1CDx)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1753-2025·2025-05-21

    PiezoWave 2 Control Unit therapeutic massager high voltage capacitor failure

    Richard Wolf GmbH is recalling 31 PiezoWave 2 Control Units (Product Number 100506US) due to a high voltage capacitor that may fail early in the device's life cycle, potentially producing smoke, burning smell, spark, or excessive heat.

    Product
    PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoelectric shockwaves (Therapeutic massager).
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1754-2025·2025-05-21

    BIB Balloon in Balloon Dilatation Catheter labeling error recalled

    Numed Inc is recalling BIB Balloon in Balloon Dilatation Catheter Model Number 420 due to incorrect labeling of balloon inflation hubs. The inner and outer balloon labels are swapped, which could lead to improper device use.

    Product
    BIB Balloon in Balloon Dilatation Catheter. Model Number: 420
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-0799-2025·2025-05-21

    Keith Valley Vanilla Flavored Ice Cream Recalled for Possible Plastic

    Wells Enterprises is recalling Keith Valley Vanilla Flavored Ice Cream 3-gallon tubs due to the possible presence of plastic foreign material in the product.

    Product
    Keith Valley Vanilla Flavored Ice Cream, 3 GAL, DISTRIBUTED BY Ben E. Keith Foods, Fort Worth, TX 76101 UPC: 046045065871, Item: 1144343
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0798-2025·2025-05-21

    Wells Enterprises French Vanilla Ice Cream Recalled for Plastic Contamination

    Wells Enterprises is recalling 17 3-gallon tubs of Artificially Flavored French Vanilla Ice Cream distributed by Sysco Corporation because plastic material may be present in the product.

    Product
    Artificially Flavored French Vanilla Ice Cream, 3 GAL, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TX 77077UPC: 00074865257275, Item: 1026416
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0788-2025·2025-05-21

    Johnny Rockets Vanilla Flavored Ice Cream Recalled for Plastic Contamination

    Wells Enterprises is recalling Johnny Rockets Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.

    Product
    Johnny Rockets Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640006564, Item: 902486
    Category
    Food
    Distribution
    0 states