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.

23351–23375 of 50435

  • HighNHTSA·20V227000·2020-04-21

    Mercedes-Benz Recalls 2020 AMG GT for eCall Wiring Defect

    Mercedes-Benz is recalling 2020 AMG GT vehicles because a missing wiring ground line may cause the emergency call system to relay inaccurate location data or prevent verbal communication with the call center.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V228000·2020-04-21

    Mercedes-Benz Recalls 2020 E 450 Coupe for Front Seatbelt Webbing Damage

    Mercedes-Benz is recalling 2020 E 450 Coupe vehicles because the front left seatbelt may contact sharp metal components, potentially damaging the webbing and reducing crash protection.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V218000·2020-04-16

    Subaru Recalls 2019 Models for Fuel Pump Failure Risk

    Subaru is recalling 2019 Impreza, Outback, Legacy, and Ascent vehicles because the low pressure fuel pump may fail, causing the engine to stall.

    Product
    SUBARU — SUBARU IMPREZA, LEGACY, ASCENT, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20734·2020-04-16

    Polaris Recalls 2019-2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard

    Polaris is recalling approximately 7,000 Model Year 2019-2020 Ranger XP 1000 and CREW XP 1000 off-road vehicles because a misrouted fuel line poses a fire hazard.

    Product
    Model Year 2019 - 2020 Ranger XP 1000 & CREW XP 1000 Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20110·2020-04-16

    MTD Southwest Recalls Troy-Bilt, Craftsman, and Remington Trimmers and Polesaws

    MTD Southwest is recalling specific Troy-Bilt, Craftsman, and Remington trimmers and polesaws because the heads can continue rotating after the throttle is released, posing a laceration hazard.

    Product
    Troy-Bilt and Craftsman 25cc 2-Cycle trimmers and Remington 25cc 2-Cycle polesaw
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20735·2020-04-16

    Polaris Recalls 2019 PRO XD and 2020 Ranger UTVs for Seat Belt Failure

    Polaris is recalling about 10,100 utility vehicles because seat belts may fail during a collision or tip-over, posing an injury hazard.

    Product
    Model Year 2019 Polaris PRO XD and model year 2020 Ranger Utility vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20111·2020-04-16

    Wyndmere Naturals Recalls Essential Oils Due to Non-Child-Resistant Packaging

    Wyndmere Naturals is recalling two essential oil products because they lack child-resistant packaging, posing a poisoning risk to young children.

    Product
    Wyndmere Birch Sweet Essential Oil and Aches and Pains Synergistic Blend
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20731·2020-04-16

    Dr. Adorable Recalls Sweet Birch Essential Oil for Packaging Defect

    Dr. Adorable is recalling Sweet Birch Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Dr. Adorable Sweet Birch Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E024000·2020-04-16

    GM Recalls Rugger Liner Tonneau Covers for 2019-2020 Trucks

    General Motors is recalling Rugger Liner hard tri-fold tonneau covers for 2019-2020 Chevrolet Silverado and GMC Sierra 1500 trucks because the attachment system may not secure the cover properly.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V217000·2020-04-16

    Ford Recalls 2020 Expedition Vehicles Due to Seatbelt Sensor Defect

    Ford is recalling 2020 Expedition vehicles because a front passenger seatbelt sensor may malfunction, potentially misclassifying the occupant and reducing crash protection.

    Product
    FORD — FORD EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2020·2020-04-15

    Radiometer ABL800 FLEX Blood Gas Analyzer Barcode Reader Recall

    Radiometer Medical ApS is recalling ABL800 FLEX analyzers because the barcode reader may misinterpret labels, potentially causing patient mixups or sample loss.

    Product
    ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1642-2020·2020-04-15

    Biomet Recalls StageOne Hip Cement Spacer Molds Due to Cleaning Concerns

    Biomet is recalling StageOne Hip Cement Spacer Molds because the cleaning process may have been insufficient or inadequately monitored.

    Product
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 64 MM, Silicone, Sterile, Item 431185.
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-0883-2020·2020-04-15

    Lindt Excellence Dark Chocolate Recalled for Undeclared Milk and Soy

    Lindt & Sprungli is recalling 174,288 bars of Excellence 85% Cocoa Dark Chocolate because they contain undeclared milk and soy.

    Product
    Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-1688-2020·2020-04-15

    Abbott Recalls Hemoglobin A1c Calibrators Due to Potential Test Bias

    Abbott Laboratories is recalling 198 kits of Hemoglobin A1c Calibrators because a manufacturing defect may cause biased patient test results outside a specific concentration range.

    Product
    "HEMOGLOBIN A1c CALIBRATORS *** REF 4P52-01 *** 307261/R03 *** S4P5X0 *** FOR USE WITH ARCHITECT" - Product Usage: use in the calibration of the Hemoglobin A1c assay.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2020·2020-04-15

    Firefly Child Seats Recalled Due to Broken Latches

    James Leckey Design Ltd is recalling Firefly child seats because of reports of broken latches.

    Product
    Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable bath seat for children aged 1-8, The GoTo Seat is a light-weight, portable, postural support seat for kids, aged between 1 and 8 with disabilities.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1641-2020·2020-04-15

    Biomet Hip Cement Spacer Mold Recalled for Cleaning Process Concerns

    Biomet is recalling StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.

    Product
    BIOMET StageOne Hip Cement Spacer Mold with Insert, 60 MM, Silicone, Sterile, Item 431184.
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Food)·F-0881-2020·2020-04-15

    Audrey's Chia Cookies Lemon Recalled for Undeclared Milk Allergen

    Health Harvest, LLC is recalling Audrey's Chia Cookies Lemon due to undeclared milk allergen. The product was distributed in Arizona and California.

    Product
    Audrey's Chia Cookies Lemon, 4 OZ flexible pouch packaging, UPC Code: 858652007010, Manufactured for Health Harvest, LLC, P.O. Box 20634, Mesa, AZ 85277. 12 pouches/case.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0880-2020·2020-04-15

    Audrey's Chia Cookies Almond Recalled for Undeclared Milk Allergen

    Health Harvest, LLC is recalling Audrey's Chia Cookies Almond because the product contains undeclared milk, a major food allergen.

    Product
    Audrey's Chia Cookies Almond, 4 OZ flexible pouch packaging, UPC Code: 858652007027, Manufactured for Health Harvest, LLC, P.O. Box 20634, Mesa, AZ 85277. 12 pouches/case.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1681-2020·2020-04-15

    Solta Medical Recalls Thermage Face Tips Due to Sparking and Burn Risk

    Solta Medical is recalling Thermage Face Tip 3.0 units because sparking during use could cause skin burns.

    Product
    Thermage Face Tip 3.0, REF/UDI: TTNS3,00C3-400/UDI (01)000850608002377; REF TTNS3.00C3-600/UDI (01)000850608002384; REF TTNS3.00C3-900; UDI (01)000850608002391 Used in dermatologic and general surgical procedures for electrocoagulation and hemostasis.
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Drugs)·D-1116-2020·2020-04-15

    Herbal Doctor Remedies Recalls Dermamycin Capsules for Unapproved New Drug Status

    Herbal Doctor Remedies is recalling Dermamycin 500mg capsules because the products are misbranded as unapproved new drugs.

    Product
    Dermamycin, 500mg Capsules, 90-count bottles, Distributed by Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Food)·F-0885-2020·2020-04-15

    Kroger Private Selection Frozen Blackberries Recalled for Norovirus Risk

    The Kroger Co is recalling Private Selection Frozen Blackberries due to potential norovirus contamination. Consumers should check their freezers for affected bags.

    Product
    PRIVATE SELECTION FROZEN BLACKBERRIES in 16 oz. bags, 10 bags per case. UPC: 0001111087809 UPC: 0001111087808
    Category
    Food
    Distribution
    31 states
  • HighFDA (Devices)·Z-1682-2020·2020-04-15

    Change Healthcare Cardiology ECG Software Recalled for Heart Rate Estimation Errors

    Change Healthcare Canada Company is recalling McKesson and Change Healthcare Cardiology ECG Management software due to potential inaccurate heart rate estimation in Sequential ECG format.

    Product
    McKesson Cardiology ECG Management, Change Healthcare Cardiology ECG Management
    Category
    Medical Device
    Distribution
    Distributed nationwide