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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8551–8575 of 113902

  • HighFDA (Food)·H-0081-2025·2025-07-02

    Nature Mills Wonderberry Leaf Soup recalled for undeclared wheat

    NatureMills US Incorporated is recalling Nature Mills Wonderberry Leaf Soup because it contains undeclared wheat allergen. Consumers with wheat allergies who purchased this product should not consume it.

    Product
    Nature Mills Wonderberry Leaf Soup, 100g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2006-2025·2025-07-02

    BD Insyte Autoguard Winged Shielded IV Catheter Needle Retraction Issue

    Becton Dickinson is recalling BD Insyte Autoguard Winged Shielded IV Catheters (Lot# 4282308) because the catheter needle may be slow to retract or fail to retract entirely following use.

    Product
    REF: 381923 BD Insyte Autoguard Winged Shielded IV Catheter, 22 GA x 1.00 in (0.9 x 25 mm) 35 mL/min, STERILEEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0065-2025·2025-07-02

    Firehook Artisan Baked Crackers Recalled for Undeclared Sesame

    Firehook of Virginia is recalling Firehook Artisan Baked Crackers Classic Sea Salt because some packages contain Everything Bagel Crackers, which include sesame that is not listed on the label.

    Product
    FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT. 8 OZ (227g) INGREDIENTS: ORGANIC WHEAT FLOUR, ORGANIC HONEY, YEAST, SALT, ORGANIC OLIVE OIL, CONTAINS: WHEAT UPC 8 99055 00063 5 FIREHOOK OF VIRGINIA, INC. CHANTILLY, VA 20151
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1999-2025·2025-07-02

    BD Insyte Autoguard Shielded IV Catheter needle retraction failure recall

    Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (REF 381423, 22GA X 1.00 IN) due to the possibility that the catheter needle may be slow to retract or fail to retract entirely.

    Product
    REF: 381423, BD Insyte Autoguard, Shielded IV Catheter, 22GA X 1.00 IN (0.9 X 25 MM) 35mL/min, STERILEEO, RxONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2008-2025·2025-07-02

    Altivate Reverse Torx Peripheral Screw labeling mismatch recall

    Encore Medical is recalling Altivate Reverse Torx Peripheral Screws because package labeling indicates a different screw size than the product actually included. This mismatch could lead to incorrect surgical implantation.

    Product
    Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 26mm Model/Catalog Number: 506-04-126 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthr
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Food)·H-0086-2025·2025-07-02

    Nature Mills Rice Papad recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Nature Mills Rice Papad (200g) because the product contains undeclared wheat allergens. Consumers with wheat allergies should not consume the affected product.

    Product
    Nature Mills Rice Papad, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2007-2025·2025-07-02

    BD Insyte Autoguard Shielded IV Catheter needle retraction failure

    Becton Dickinson is recalling BD Insyte Autoguard Shielded IV Catheters (20 GA x 1.16 in, REF 381434) because the catheter needle may be slow to retract or fail to retract entirely.

    Product
    REF: 381434 BD Insyte Autoguard Shielded IV Catheter, 20 GA x 1.16 in (1.1 x 30 mm) 60 mL/min, STERILEEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0077-2025·2025-07-02

    Nature Mills Horsegram Rice Mix recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Nature Mills Horsegram Rice Mix (200g) due to undeclared wheat allergens. The product was distributed via the firm's website throughout the USA.

    Product
    Nature Mills Horsegram Rice Mix, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0078-2025·2025-07-02

    NatureMills Avarampoo Soup recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling NatureMills Avarampoo Soup (100g) because the product contains wheat that is not declared on the label, posing a risk to consumers with wheat allergies.

    Product
    NatureMills Avarampoo Soup, 100g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0058-2025·2025-07-02

    Madeline's Patisserie Chocolate Croissants recalled for undeclared wheat

    Element 112, LLC is recalling Madeline's Patisserie Chocolate Croissants due to undeclared wheat. Consumers with wheat allergies could be at risk.

    Product
    1) Madeline's Patisserie 2.5 ounce Chocolate Croissant, Net Wt. 3 lbs. 8 oz. (1,587.6g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case 2) Madeline's Patisserie 3.5 ounce Chocolate Croissant, Net Wt. 4 lbs. 11 oz. (2,126.2g), pack
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0083-2025·2025-07-02

    Nature Mills Traditional Rasam Powder recalled for undeclared allergens

    NatureMills US Incorporated is recalling Nature Mills Traditional Rasam Powder (200g) because it contains undeclared sesame and wheat allergens that are not listed on the label.

    Product
    Nature Mills Traditional Rasam Powder, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0073-2025·2025-07-02

    NatureMills Dal Garlic Rice Mix 200g Recall for Undeclared Allergens

    NatureMills US Incorporated is recalling NatureMills Dal Garlic Rice Mix, 200g, because the product contains undeclared milk and wheat allergens that are not listed on the label.

    Product
    NatureMills Dal Garlic Rice Mix, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0079-2025·2025-07-02

    Nature Mills Horsegram Soup recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Nature Mills Horsegram Soup 100g packets because they contain undeclared wheat, a major allergen. The product was distributed nationally via the company's website.

    Product
    Nature Mills Horsegram Soup, 100g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2000-2025·2025-07-02

    BD Insyte Autoguard BC Winged IV Catheter Needle Retraction Issue

    Becton Dickinson is recalling a specific lot of BD Insyte Autoguard BC Winged IV catheters (REF 382633, Lot 4222721) due to reports that the catheter needle may be slow to retract or fail to retract entirely.

    Product
    REF: 382633, BD Insyte Autoguard BC Winged, Shielded IV Catheter with Blood Control Technology, 20GA x 1.00 in (1.1x25 mm) 63 mL/min, STERILEEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2029-2025·2025-07-02

    GE Healthcare LOGIQ F R3 Ultrasound System Incorrect Fetal Weight Data Display

    GE Healthcare is recalling the LOGIQ F R3 ultrasound system because it may display previous obstetric patient data in fetal weight measurements, potentially leading to incorrect clinical decisions about fetal size and growth.

    Product
    GE Healthcare LOGIQ F R3 Ultrasound System, Model/Catalog Number 5943263, diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0087-2025·2025-07-02

    Nature Mills Black Kavuni Porridge Mix recalled for undeclared wheat

    NatureMills US Incorporated is recalling Nature Mills Black Kavuni Porridge Mix (200g) because it contains undeclared wheat allergens. Consumers with wheat allergies should not consume this product.

    Product
    Nature Mills Black Kavuni Porridge Mix, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1997-2025·2025-07-02

    Bigfoot Unity Diabetes Management System Pen Caps Unresponsive Due to Firmware Error

    Bigfoot Biomedical is recalling Bigfoot Unity Diabetes Management System Pen Caps due to a firmware issue that may cause insulin pens to become unresponsive. People with diabetes may lack information needed to make timely treatment decisions.

    Product
    Bigfoot Unity Diabetes Management System SW-300689-01 Bigfoot Inject v1 Pen Cap LCAP Firmware 1.3.0 Release Configuration, Rev H SW-300689-02 Bigfoot Inject v1 Pen Cap RCAP Firmware 1.3.0 Release Configuration, Rev H The Bigfoot Unity Diabetes Management System that include the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2034-2025·2025-07-02

    Philips Spectral CT Computed Tomography X-ray System Software

    Philips Spectral CT systems with affected software may experience unintended motion of the gantry or table that could lead to contact with operators or patients. Additional software issues may also affect CT performance.

    Product
    Spectral CT. Computed tomography X-ray system.
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2018-2025·2025-07-02

    CDI OneView System BPM Probe temperature sensor measurement inaccuracy

    Terumo Cardiovascular Systems is recalling CDI OneView System BPM Probe units due to thermistor assembly errors that cause inaccurate temperature and blood gas measurements, potentially leading to inappropriate clinical decisions.

    Product
    CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI OneView BPM Probe Trial Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2002-2025·2025-07-02

    BD Insyte Autoguard Shielded IV Catheter needle retraction defect

    Becton Dickinson is recalling one lot of BD Insyte Autoguard Shielded IV Catheters (REF 381433, 20GA x 1.00 in) due to reports that the catheter needle may retract slowly or fail to retract completely.

    Product
    REF: 381433, BD Insyte Autoguard Shielded IV Catheter, 20GA x 1.00 in (1.1x25 mm) 65 mL/min, STERILEEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2025·2025-07-02

    PRIMA 4MM Eccentrical Adaptor With Screw Medical Device Recall

    Limacorporate S.p.A is recalling PRIMA 4MM Eccentrical Adaptor with Screw devices because the black laser marking used to identify positioning may be missing. The defect could affect proper device placement during use.

    Product
    PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0071-2025·2025-07-02

    Idly Chili Powder 200g recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Idly Chili Powder 200g because it contains undeclared wheat, a common allergen that poses a risk to consumers with wheat allergies.

    Product
    Idly Chili Powder 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2003-2025·2025-07-02

    BD Insyte Autoguard BC Pro IV Catheter Needle Retraction Defect

    Becton Dickinson is recalling BD Insyte Autoguard BC Pro Winged Shielded IV Catheters (REF 382944) due to reports that the catheter needle may retract slowly or fail to retract completely.

    Product
    REF: 382944, BD Insyte Autoguard BC Pro Winged Shielded IV Catheter, 18 GA x 1.16 in (1.3 x 30 mm) 95 mL/min, STERILEEO, RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0080-2025·2025-07-02

    Nature Mills Moringa Leaf Soup recalled for undeclared wheat

    NatureMills US Incorporated is recalling Nature Mills Moringa Leaf Soup (100g) distributed via its website due to undeclared wheat allergens that may pose a risk to consumers with wheat allergies or sensitivities.

    Product
    Nature Mills Moringa Leaf Soup, 100g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0074-2025·2025-07-02

    NatureMills Moringa Rice Mix recalled for undeclared wheat

    NatureMills US Incorporated is recalling NatureMills Moringa Rice Mix (200g) because it contains undeclared wheat allergens. Consumers with wheat allergies should not consume the product.

    Product
    NatureMills Moringa Rice Mix, 200g
    Category
    Food
    Distribution
    0 states