The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

4176–4200 of 52939

  • HighCPSC·25371·2025-07-03

    Hyper Tough, Worx, and Portland Electric Chainsaws and Pole Saws Recall

    Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.

    Product
    Hyper Tough, Worx and Portland Chainsaws and Pole Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25369·2025-07-03

    Trane and American Standard Gas-Electric Packaged Units Recalled for Gas Leak Risk

    Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.

    Product
    Trane and American Standard Gas/Electric Packaged Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25374·2025-07-03

    509 Helmets Recalled Due to Risk of Head Injury

    509 helmets and 509 for Polaris helmets may fail to provide sufficient protection in a crash. One incident reported a helmet detachment during a crash resulting in a concussion.

    Product
    509 helmets and 509 for Polaris helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2001-2025·2025-07-02

    BD Insyte Autoguard Winged IV Catheter needle retraction failure recall

    Becton Dickinson is recalling BD Insyte Autoguard Winged IV Catheters (Ref. 381533, Lot 4282452) because the catheter needle may be slow to retract or fail to retract entirely.

    Product
    REF: 381533, BD Insyte Autoguard Winged, Shielded IV Catheter, 20 GA x 1.00 in (1.1 x 25 mm) 65mL/min, STERILEEO,RxOnly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Food)·H-0076-2025·2025-07-02

    Nature Mills Vallarai Rice Mix recalled for undeclared wheat allergen

    NatureMills US Incorporated is recalling Nature Mills Vallarai Rice Mix (200g) because it contains undeclared wheat allergen. The product was distributed throughout the USA via the firm's website.

    Product
    Nature Mills Vallarai Rice Mix, 200g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2017-2025·2025-07-02

    BD Pyxis Dispensing Cabinet Software Configuration Error Medical Device Recall

    CareFusion is recalling BD Pyxis automated dispensing cabinets and related devices due to a software configuration issue that can prevent user access to the medication dispensing application. This may delay patient care when Microsoft patches are installed during system upgrades.

    Product
    Product Name [REF]: Supply Server, CCE Enterprise SW Site License (2-5), BD Pyxis Logistics [806], BD Pyxis MedStation 4000 Main 10885403512629 [303], BD Pyxis MedStation ES Tower 10885403512674 [352], BD Pyxis Anesthesia Station ES 10885403477836 [327], BD Pyxis MedStation ES (M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Devices)·Z-2030-2025·2025-07-02

    GE Healthcare Versana Ultrasound Systems display incorrect fetal weight data

    GE Healthcare Versana Premier R3 and LOGIQ F R3 ultrasound systems can display previous obstetric patient data in fetal weight measurement reports, potentially leading to incorrect clinical decisions based on inaccurate fetal size and growth calculations.

    Product
    GE Healthcare Versana Ultrasound Systems, sold under the following names and Model/Catalog Numbers: 1) Versana Premier R3 VS, Model/Catalog Number 5938558; 2) Versana Premier R3 VA, Model/Catalog Number 5938559; 3) Versana Premier Lotus 4PP, Model/Catalog Number 5938560;
    Category
    Medical Device
    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 (Devices)·Z-2028-2025·2025-07-02

    REMISOL Advance Medical Device Software Defect Affecting Reference Range Calculations

    A software issue in REMISOL Advance may incorrectly process date-of-birth information from laboratory systems, causing incorrect reference range calculations and potentially auto-validating erroneous test result flags. The actual test results are not changed, but their evaluation may be affected.

    Product
    REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487; B92488; C24317; C28652; C37500; D04164; C44703; C57017; C69412; C69413; C73942; C73941; C88470; C88471 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 con
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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 (Devices)·Z-2024-2025·2025-07-02

    PRIMA 2MM Eccentrical Adaptor With Screw Sterile Medical Device

    Limacorporate is recalling PRIMA 2MM Eccentrical Adaptor With Screw sterile devices because the black laser marking used to identify position may be missing.

    Product
    PRIMA 2MM ECCENTRICAL ADAPTOR WITH SCREW REF: 1367.15.702, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-1994-2025·2025-07-02

    Barco NexxisOR System Display Encoders and Decoders Recalled

    Barco N.V. is recalling certain NexxisOR system display encoder and decoder models due to duplicate MAC addresses that can cause system malfunction, audio/video interruptions, and delayed procedures when multiple units are deployed together.

    Product
    Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; comp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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 (Food)·H-0084-2025·2025-07-02

    Nature Mills Garlic Vadam 100g Recalled for Undeclared Wheat

    NatureMills US Incorporated is recalling Nature Mills Garlic Vadam (100g) distributed nationwide via its website because the product contains undeclared wheat allergens.

    Product
    Nature Mills Garlic Vadam, 100g
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·25V409000·2025-07-02

    Polestar 2 May Lose Brake Function While Using One Pedal Drive

    Certain 2021 and 2024 Polestar 2 vehicles may lose brake function while coasting downhill and using One Pedal Drive mode. Polestar will provide a free over-the-air software update to fix the control module defect.

    Product
    POLESTAR — POLESTAR POLESTAR 2
    Category
    Vehicle
    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 (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 (Food)·H-0075-2025·2025-07-02

    NatureMills Curry Leaf Rice Mix recalled for undeclared wheat

    NatureMills US Incorporated is recalling NatureMills Curry Leaf Rice Mix (200g) because it contains undeclared wheat, which poses a risk to consumers with wheat allergies.

    Product
    NatureMills Curry Leaf Rice Mix, 200g
    Category
    Food
    Distribution
    0 states
  • 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 (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