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.

1026–1050 of 52929

  • HighFDA (Devices)·Z-2193-2026·2026-05-20

    Daig Livewire Steerable Electrophysiology Catheter Sterile Seal Defect Recall

    Stryker Sustainability Solutions is recalling three lots of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile packaging. The defect affects units distributed in the US, Israel, and Canada.

    Product
    Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V319000·2026-05-20

    Blue Bird Recalls 2027 Vision School Buses Due to Wheelchair Retract Defect

    Blue Bird is recalling 2027 Vision school buses because wheelchair retractors may fail to lock. This defect could allow wheelchairs to move during transit, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2165-2026·2026-05-20

    Dexcom ONE+ iOS CGM App Software Defect Delayed Glucose Alerts

    Dexcom, Inc. is recalling Dexcom ONE+ iOS CGM App versions 1.5.0 and 1.6.0 due to a software defect that can delay glucose alerts and notifications, risking delayed detection of low or high blood sugar events.

    Product
    Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring Syste
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2169-2026·2026-05-20

    QuickVue Dipstick Strep A Test Recalled for False Positive Results

    Quidel Corporation is recalling the QuickVue Dipstick Strep A Test (50T, REF 20108) due to the potential for false positive results. The product was distributed nationwide.

    Product
    QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V313000·2026-05-18

    2026 Keystone Alpine recreational trailers recalled for loose shock bolts

    Keystone RV Company is recalling certain 2024–2026 recreational trailers because shock bolts may have been incorrectly tightened, which could cause loss of vehicle stability and increase crash risk.

    Product
    KEYSTONE — KEYSTONE COUGAR, ALPINE, WALKABOUT, MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V316000·2026-05-18

    2025–2026 Hyundai Tucson and Santa Cruz Front Camera Software Issue

    Hyundai is recalling certain 2025 and 2026 Tucson, Tucson Hybrid, Tucson PHEV, and Santa Cruz vehicles due to front camera software that may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI TUCSON, TUCSON PLUG-IN HYBRID, SANTA CRUZ, TUCSON HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V310000·2026-05-15

    Altec Recalls Aerial Devices Due to Emergency Stop Failure

    Altec is recalling specific aerial device vehicles because the ground-level emergency stop may fail to halt hydraulic functions in ePTO mode, increasing injury risk.

    Product
    ALTEC — ALTEC AM SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE, LR SERIES AERIAL DEVICE, AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26480·2026-05-14

    Superbobi Pool Drain Covers Recalled for Entrapment and Drowning Risk

    Superbobi 7 3/8-inch pool drain covers violate federal safety standards and pose entrapment and drowning hazards. Pool owners should stop using affected covers immediately.

    Product
    Superbobi 7 3/8 Inch Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26488·2026-05-14

    Petzl America Recalls Three Climbing Harness Models for Fall Hazard

    Petzl America is recalling about 29,300 climbing harnesses because the D-ring attachment point can release, creating a risk of serious injury or death from a fall.

    Product
    Petzl ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V308000·2026-05-14

    Hyundai Elantra Hybrid power control units may overheat

    Hyundai is recalling certain 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit assembly may overheat, increasing the risk of a fire. 54,337 vehicles are affected.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V306000·2026-05-14

    Honda Prologue and Acura ZDX rearview cameras may display distorted images

    Honda is recalling certain 2024-2025 Prologue and 2024 Acura ZDX vehicles because the rearview camera screen may display a distorted or blank image. 59,887 vehicles are affected.

    Product
    ACURA — ACURA, HONDA ZDX, PROLOGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26484·2026-05-14

    LiCB CR2032 Lithium Coin Batteries Recalled for Child-Resistant Packaging Violation

    Guangzhou Lichengbei Battery Technology Co., Ltd. (LiCB) has recalled about 94,000 CR2032 3V lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Ingestion can cause serious internal injuries, chemical burns, and death.

    Product
    LiCB CR2032 3V Lithium Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26489·2026-05-14

    Electric Water Kettles Recalled Due to Burn Hazard from Loosening Handle

    ZWILLING J.A. Henckels has recalled approximately 113,440 ENFINIGY electric kettles in the U.S. because the handle can loosen and separate, causing hot water to spill and posing a burn injury risk.

    Product
    Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26487·2026-05-14

    Petzl Climbing and Adventure-Park Harnesses Recalled for Fall-Hazard Risk

    Petzl America is recalling about 1,270 SIMBA and SWAN EASYFIT harnesses because missing rivets in the buckles can cause them to open, creating a risk of serious injury or death from falls.

    Product
    Petzl SIMBA CLIMBING and SIMBA PARK Children's Harnesses, SWAN EASYFIT STEEL and SWAN EASYFIT STAINLESS Harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0744-2026·2026-05-13

    Loard's pecan praline ice cream has undeclared milk and pecans

    Loard's Pecan Praline Ice Cream in 32 oz tubs is being recalled because milk and pecans are undeclared on the label. 875 units are affected.

    Product
    Loard's Pecan Praline Ice Cream - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0724-2026·2026-05-13

    Loard's champagne sherbert has undeclared milk and Red #40

    Loard's Champagne Sherbert in 32 oz tubs is being recalled because milk and Red #40 are undeclared on the label. 188 units are affected.

    Product
    Loard's Champagne Sherbert - 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0706-2026·2026-05-13

    Walker Honey Hatch creamed honey may contain metal and plastic fragments

    Hatch Creamed Honey from Walker Honey Co is being recalled because it may contain stainless steel dust or flakes and small particles or shreds of plastic.

    Product
    Hatch Creamed Honey 671333101339 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey. The UPC codes remained the same. Packaged in Glass jars UPC Code: 6
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·26E030000·2026-05-13

    Hale Recalls Weldon UV800 Display Units for Emergency Equipment Failure

    Hale Products Inc is recalling Weldon UV800 Display Units that may fail to power on or respond to touch, preventing the activation of emergency lights and firefighting equipment.

    Product
    EQUIPMENT:EMERGENCY:FIRE SUPRESSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0512-2026·2026-05-13

    DELFLEX Peritoneal Dialysis Solution bags recalled for sterility risk

    Fresenius Medical Care is recalling DELFLEX Dextrose Peritoneal Dialysis Solution bags due to potential leaks from perforations that may compromise sterility. The recall affects 37,215 bags distributed nationwide.

    Product
    DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only, 1.5% DEX. LM/LC, 2L 5PK, Part Number 054-20221, Fresenius Medical Care North America, 920 Winter Street, Waltham, MA 02451.
    Category
    Drug
    Distribution
    Distributed nationwide