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.

25376–25400 of 50447

  • HighNHTSA·19V551000·2019-07-25

    Alfa Romeo Giulia and Stelvio Recalled for Inaccurate Fuel Level Display

    FCA US LLC is recalling 2018-2019 Alfa Romeo Giulia and Stelvio vehicles because the Body Control Module may display a fuel level higher than the actual amount, increasing the risk of a crash.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1983-2019·2019-07-24

    Olympus Mobile Workstations Recalled for Potential Instability

    Olympus is recalling WM-NP2 and WM-DP2 mobile workstations because the control panel arm may cause the unit to fall over if a heavy monitor is attached.

    Product
    Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2019·2019-07-24

    DeRoyal Custom Surgical Packs Recalled for Sterility Barrier Defect

    DeRoyal is recalling 108 custom surgical packs in Oklahoma because they contain defective Cardinal Health Blunt Cannulas that could compromise sterility.

    Product
    DeRoyal THE RESOURCE GROUP, CRANI PACK, REF 89-9211.07 custom surgical pack
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1553-2019·2019-07-24

    Sprouts Farmers Market Cut Leaf Spinach Recalled for Listeria

    Sprouts Farmers Market is recalling 1,046 cases of Cut Leaf Spinach because testing revealed the presence of Listeria monocytogenes.

    Product
    Sprouts Farmers Market Cut Leaf Spinach, Net Wt 16 Oz (1 lb), 453 g, Manufactured exclusively for Sprouts Farmers Market, Phoenix, AZ UPC 8 74875 00982 2, packaged in plastic bags, 12 bags per case.
    Category
    Food
    Distribution
    19 states
  • HighCPSC·19173·2019-07-24

    Trek Recalls Kickster Bikes Due to Broken Steer Tube Clamp Hazard

    Trek is recalling Kickster balance bikes because the steer tube clamp can break, posing a fall hazard to children. Consumers should take bikes to a retailer for a free repair.

    Product
    Trek Kickster
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1951-2019·2019-07-24

    GE Healthcare Recalls Revolution CT Scanners Due to Radiation Exposure

    GE Healthcare is recalling Revolution CT scanners because they may expose patients to additional low-dose radiation.

    Product
    Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2019·2019-07-24

    DJO Aircast Sterile Cuff Recall Due to Sterility Concerns

    DJO, LLC is recalling 9 units of Aircast REF 3011 sterile cuffs because they may not meet sterility requirements.

    Product
    Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·19V545000·2019-07-24

    Mercedes-Benz Metris Recalled for Incorrect Operator's Manual

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because the printed operator's manual may not match the vehicle's features, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1550-2019·2019-07-24

    Oregon Potato Company Recalls Frozen Red Raspberries Due to Norovirus Risk

    Oregon Potato Company is recalling 2,970 cases of frozen whole red raspberries due to potential Norovirus contamination. The product was distributed across ten western and central US states.

    Product
    Frozen whole Red Raspberries; packed in a 12 oz. polyethylene bag; UPC: 0 70552 30501 4. The label is read in parts: "***WinCo Foods Red Raspberries *** KEEP FROZEN***PRODUCT OF USA***DISTRIBUTED BY: WINCO FOODS LLC, BOISE, ID***".
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1967-2019·2019-07-24

    BD Microtainer Tubes Recalled Due to Reduced Anticoagulant Additive

    Becton Dickinson is recalling specific Microtainer tubes because they may contain reduced or no additive, causing blood samples to clot and delaying test results.

    Product
    BD Microtainer Tube w/ BD Microgard Closure, K2EDTA additive, Model Numbers 365974 and 365975 Product Usage: The Microtainer¿ Brand Tube with EDTA(K2) Reorder No. 365974, is used to collect, anticoagulate, transport and store skin puncture blood specimens for testing the…
    Category
    Medical Device
    Distribution
    16 states
  • HighNHTSA·19V549000·2019-07-24

    Thomas Built Buses Recall Roof Escape Hatch Handle Defect

    Daimler Trucks North America is recalling specific Thomas Built Buses because the roof escape hatch handle may break, preventing emergency exit.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1960-2019·2019-07-24

    Zimmer Biomet Recalls Reverse Shoulder Instrument Cases Due to Sterilization Validation

    Zimmer Biomet is recalling 92 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.

    Product
    Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1961-2019·2019-07-24

    Zimmer Biomet Recalls Reverse Shoulder Instrument Cases Due to Sterilization Validation

    Zimmer Biomet is recalling 1,257 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.

    Product
    Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1608-2019·2019-07-24

    Kroger Stuffed Mushrooms Recalled for Undeclared Soy Allergen

    GH Foods is recalling Kroger Stuffed Mushrooms because the product contains soy, which is not declared on the label.

    Product
    Kroger Stuffed Mushrooms; Net Wt. 7 oz. (193 g) over-wrapped tray Perishable, Keep Refrigerated. Cook before consumption UPC: 2676614086 Distributed by Renaissance Food Group, LLC. 1730 Eastbridge Ave. Riverside, CA 92507
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1986-2019·2019-07-24

    Clariance Erisma-LP Posterior Fixation System Recalled for Screw Disassembly Risk

    Clariance Inc is recalling Erisma-LP posterior fixation system components due to a potential for polyaxial screws to disassemble during implantation.

    Product
    Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws - 4.5, 5.5, 6.5, 7.5, 8.5, 9.5, 105 mm (all lengths); 2. Erisma-LP Screwdriver; 3. Erisma-LP T20 Wrench; 4. Erisma-LPT20 Snap Fit Tightening…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1971-2019·2019-07-24

    Electrode Conductivity Spray Solution Recalled for Antimicrobial Testing Failures

    Pharmaceutical Innovations, Inc. is recalling ElectroMist Electrode Conductivity Spray Solution due to potential failures in stability antimicrobial effectiveness testing.

    Product
    ElectroMist product codes: 36-3310-04 - Product Usage: Electrode Conductivity Spray Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1972-2019·2019-07-24

    Pharmaceutical Innovations Recalls Alpha Conducting Solution Due to Stability Testing Concerns

    Pharmaceutical Innovations, Inc. is recalling Alpha Conducting solution due to potential failures in stability antimicrobial effectiveness testing. The product was distributed in the US and internationally.

    Product
    Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V542000·2019-07-24

    Forest River Recalls 2019 Glaval and Startrans Buses for Seat Belt Bolt Issue

    Forest River is recalling 2019 Glaval and Startrans buses because driver's seat belt anchor bolts may not be fully tightened, potentially causing the seat belt to fail in a crash.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS COMMUTE, PRIMETIME, CONCORDE II, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1965-2019·2019-07-24

    GE Healthcare Recalls Two Ultrasound Systems Due to Transducer Misalignment

    GE Healthcare is recalling two ultrasound systems because transvaginal probes may be misaligned. The devices were distributed in the US and internationally.

    Product
    Repair RIC5-9A-RS System, imaging, pulsed doppler, ultrasonic and Refurbish RIC-5-9-D REALTIME 4D
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·19V547000·2019-07-24

    Audi Recalls Vehicles Due to Passenger Air Bag Disabling Risk

    Audi is recalling 2017-2019 models because cable oxidation may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A5, A4 ALLROAD, RS 5, S5 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1973-2019·2019-07-24

    SpineFrontier Recalls A-CIFT SoloFuse Fixed Angle Driver Due to Binding Risk

    SpineFrontier, Inc. is recalling six A-CIFT SoloFuse Fixed Angle Drivers because they may bind when advancing fixation screws.

    Product
    A-CIFT SoloFuse Fixed Angle Driver, Model Number 13-32101-01 (Component Part Numbers 14-32107-01 and 14-32106)
    Category
    Medical Device
    Distribution
    4 states