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.

19676–19700 of 50413

  • HighNHTSA·21V621000·2021-08-09

    Travel Trailers Recalled for Fresh Water Tank Securement Defect

    Forest River is recalling certain 2019-2021 travel trailers because the fresh water tank may not be properly secured to the frame. A detached tank could increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V619000·2021-08-06

    Hyundai Recalls Sonata, Accent, Azera, and Sonata Hybrid for Trunk Latch Defect

    Hyundai is recalling specific 2016-2020 Sonata, Sonata Hybrid, Accent, and Azera vehicles because a damaged trunk latch may prevent opening from the inside, risking entrapment.

    Product
    HYUNDAI — HYUNDAI SONATA, SONATA HYBRID, AZERA, ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V616000·2021-08-06

    2021 Volkswagen Atlas Relays Pose Fire Risk, Recall Issued

    Volkswagen is recalling 2021 Atlas and Atlas Cross Sport vehicles with damaged relays that may activate the horn or starter indefinitely, creating a fire hazard. Dealers will replace affected relays free of charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V615000·2021-08-06

    2022 Volkswagen Taos Engine Stall Software Defect Recall

    Volkswagen recalls 2022 Taos all-wheel-drive vehicles for a software defect that may cause engine stall when stopping, increasing crash risk. Dealers will update the engine control unit software free of charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V613000·2021-08-05

    2021 Maserati Tire Placard Recall: Incorrect Pressure Information

    Maserati is recalling certain 2021 Ghibli and Quattroporte vehicles with 21-inch tires due to incorrect tire pressure information on the placard. Improper tire inflation could affect vehicle stability and control.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V612000·2021-08-05

    2022 Chevrolet Equinox and Terrain tire recall for tread separation risk

    General Motors is recalling 2021-2022 Chevrolet Equinox and GMC Terrain vehicles with certain Hankook tires that may have insufficient curative agent, risking tread separation and loss of vehicle control.

    Product
    CHEVROLET — CHEVROLET, GMC EQUINOX, TERRAIN, TERRAIN NA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V611000·2021-08-05

    Cadillac CT4 and CT5 roof rail air bags installation defect

    General Motors is recalling 2020-2022 Cadillac CT4 and CT5 vehicles because roof rail side-curtain air bags may not have been installed correctly. Improper installation could prevent proper deployment during a crash.

    Product
    CADILLAC — CADILLAC CT4, CT5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V606000·2021-08-05

    2021 Audi RS Q8 rear seat belt retractors may deactivate prematurely

    Certain 2021 Audi RS Q8 vehicles have rear seat belt retractors that may deactivate prematurely, preventing child restraint systems from securing properly. Dealers will repair affected components free of charge.

    Product
    AUDI — AUDI, VOLKSWAGEN Q8, A6, A4, A5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2021·2021-08-04

    OEC Elite Mobile C-Arm Recalled for Battery Depletion

    GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.

    Product
    OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2159-2021·2021-08-04

    Medtronic Vectris SureScan MRI lead kits recalled for incorrect labeling

    Medtronic Neuromodulation is recalling 1131 units of Vectris SureScan MRI lead kits with incorrect electrode spacing information on packaging labels. This could affect proper device installation.

    Product
    Medtronic Vectris SureScan MRI, Catalog Numbers: a) 977A260 b) 977A275 c) 977A290
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2151-2021·2021-08-04

    CooperVision Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling MEDIFLEX ELITE 1 DAY TORIC daily disposable contact lenses (lot W0106167) due to misaligned axis marks that can cause blurred vision.

    Product
    MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2155-2021·2021-08-04

    Proteus 235-Proton Therapy System May Deliver Unintended Radiation

    The Proteus 235-Proton Therapy System may deliver proton therapy without prescribed beam gating if the user forgets to select the trigger input. This could cause radiation to be positioned incorrectly.

    Product
    Proteus 235-Proton Therapy System
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·21V608000·2021-08-04

    2021 Porsche Taycan Seat Belt Retractor Defect May Prevent Child Restraint Securing

    Porsche is recalling certain 2021 Taycan models because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly during a crash.

    Product
    PORSCHE — PORSCHE 911, PANAMERA 4S, PANAMERA 4 E-HYBRID, PANAMERA TURBO S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0818-2021·2021-08-04

    f'real Made to Order Shake Base Recalled for Undeclared Milk

    Rich Products Corp is recalling f'real Made to Order Shake Base because the outer label incorrectly identifies the product as "Smoothie Base," failing to disclose the presence of milk. Consumers with milk allergies or sensitivities face a potential health risk.

    Product
    f'real Made to Order Shake Base - 8 fl oz (237ml) cups Out packaging may read 'Smoothie-base' Lid may read ' Shake-base' 12 individual cups packed into a shrink-wrapped pulp tray
    Category
    Food
    Distribution
    5 states
  • HighCPSC·21174·2021-08-04

    Two Million Dehumidifiers Recalled for Fire and Burn Hazards

    About 2 million dehumidifiers manufactured by New Widetech under multiple brand names are recalled because they can overheat and catch fire, posing fire and burn hazards. Consumers should stop using them immediately.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2150-2021·2021-08-04

    Contact lens recall: misaligned axis mark may cause blurred vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that may cause blurred vision. The recall affects 450 lenses distributed across select U.S. states and multiple countries.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2021·2021-08-04

    CLARITI 1 DAY TORIC Contact Lenses Recalled Due to Axis Mark Misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected patients should discontinue use and contact their eye care provider.

    Product
    CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0804-2021·2021-08-04

    Randall Garbanzo Beans Recall: Defective Temperature Monitoring Devices

    Randall Foods is recalling Randall Garbanzo Beans in 24oz and 15.4oz glass jars due to non-functioning temperature indicating devices in retorts, which may affect proper food safety processing.

    Product
    RANDALL GARBANZO BEANS 24OZ glass jars UPC 070095000711; RANDALL GARBANZO BEANS 15.4OZ glass jars UPC 070095000735
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-2144-2021·2021-08-04

    Contact Lens Axis Mark Misalignment May Cause Blurred Vision

    CooperVision's AQUATECH PLUS 1 DAY TORIC contact lenses (lot R0121629) have misaligned axis marks that may cause blurred vision in patients.

    Product
    AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2163-2021·2021-08-04

    Coaxial Interventional Needles recalled for potential sterilization failure

    Coaxial Interventional Needles from INNOVATIVE TOMOGRAPHY PRODUCT GMBH may not be properly sterilized. Multiple lot numbers are affected and should not be used.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2140-2021·2021-08-04

    Heater Cooler Unit Recall Due to Potential Bacterial Contamination Risk

    Maquet Medical Systems USA is recalling 33 Heater Cooler Unit (HCU 30) devices due to potential water contamination in device circuits that could introduce Mycobacteria or other bacteria. The devices were distributed to nine U.S. states.

    Product
    Heater Cooler Unit (HCU 30) The device supplies temperature-controlled water for cardioplegia heat exchangers and for blood heat exchangers in extracorporeal circulation and for blankets with which patients can be warmed or cooled.
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·21E071000·2021-08-04

    Enerco Propane Regulators Recalled Due to Fire Risk

    Enerco Group is recalling specific propane regulators that may fail, causing excessive gas pressure and increased fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis mark misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC daily disposable contact lenses due to misaligned axis marks that can cause blurred vision. Affected lenses in lot U0108833 were distributed in seven US states and internationally.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide