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.

21651–21675 of 50426

  • HighNHTSA·20V726000·2020-11-20

    2021 Lincoln Aviator steering knuckle defect increases crash risk

    Ford is recalling certain 2021 Lincoln Aviator vehicles due to improperly manufactured steering knuckles that may fracture, reducing steering control and increasing crash risk. Dealers will inspect and replace affected knuckles free of charge.

    Product
    LINCOLN — LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V719000·2020-11-20

    Newmar Motorhomes Recalled for Cooking Stove Gas Leak Fire Risk

    Newmar motorhomes equipped with Dometic 3-burner cooking stoves may have an overtightened saddle valve bolt that damages the seal, causing a gas leak and increasing fire risk. Owners should contact Newmar for a free remedy.

    Product
    NEWMAR — NEWMAR VENTANA, VENTANA LE, BAY STAR, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V718000·2020-11-19

    2021 Thor Motor Coach Four Winds motorhomes recalled for stove gas leak

    Thor Motor Coach is recalling certain 2021 Four Winds motorhomes with Dometic stoves due to a potential gas leak that could increase fire risk. The stove's saddle valve bolt may be overtightened, damaging the seal.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21709·2020-11-19

    Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Clutch Failure Hazard

    Polaris is recalling about 18,400 RZR recreational off-highway vehicles because the clutch can fail, posing an injury hazard. No injuries have been reported.

    Product
    Model Years 2020-2021 RZR PRO XP, PRO XP4 and Model Year 2021 RZR Turbo S, Turbo S4, XP Turbo and XP 4 Turbo ROV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0439-2021·2020-11-18

    Fresenius Liberty Select Cycler Software Recall for Inadequate Dialysis Risk

    Fresenius Medical Care is recalling Liberty Select Cycler devices with software version 2.9.0 because a software error may cause the device to fail to recognize extra fluid, potentially leading to inadequate dialysis.

    Product
    Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0446-2021·2020-11-18

    United Imaging uCT 550 CT Scanners Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 550 CT scanners because an incorrect delay timer display may expose operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 550, Rx, CE, GTIN: 06971576831036 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0445-2021·2020-11-18

    United Imaging uCT 530 CT Scanner Recalled for Incorrect Timer Display

    Shanghai United Imaging Healthcare Co., Ltd. is recalling four uCT 530 CT scanners because an incorrect delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0427-2021·2020-11-18

    Boston Scientific AMS 700 MS Pump Recall for Activation Difficulties

    Boston Scientific is recalling AMS 700 MS Pumps due to reports of difficulty activating the device to inflate cylinders.

    Product
    AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0447-2021·2020-11-18

    United Imaging uCT 760 CT Scanner Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 760 CT scanners because a display error may cause operators to receive unnecessary radiation exposure.

    Product
    Computed Tomography X-Ray System, Model uCT 760, Rx, CE, GTIN: 06971576831043 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0094-2021·2020-11-18

    Wolfgang Confectioners Recalls Hu Almond Hunks Due to Undeclared Cashews

    Wolfgang Confectioners is recalling Hu Almond Hunks because cashews were found in the almond product pouches, posing a mislabeling hazard.

    Product
    Hu Almond Hunks, Almonds + Sea Salt Chocolate Covered Hunks 4 oz., stand up pouch, 6 bags per case .
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0428-2021·2020-11-18

    Quidel SARS Antigen Test Kits Recalled for False Positive Results

    Quidel is recalling 8,628 SARS Antigen FIA test kits due to false positive results. The affected units were distributed to 24 U.S. states.

    Product
    QUIDEL Sofia SARS Antigen FIA IVD REF 20374
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0448-2021·2020-11-18

    United Imaging uMI 550 PET/CT System Recalled for Incorrect CT Scan Delay Timer

    Shanghai United Imaging Healthcare is recalling nine uMI 550 PET/CT systems because an incorrect CT scan delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Positron Emission Tomography and Computed Tomography System, Model uMI 550, Rx, CE, GTIN: 06971576832026 - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0432-2021·2020-11-18

    Inpeco FlexLab Automation System Recalled for Potential Sample Dilution

    Inpeco S.A. is recalling 93 FlexLab Automation Systems with Aliquoter Modules because a software error may cause samples to be diluted with water, leading to erroneous test results.

    Product
    FlexLab (FLX) Automation System with the Aliquoter Module (Inpeco P/N FLX-212) The FlexLab (aka Accelerator a3600 and Aptio Automation) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0443-2021·2020-11-18

    Maquet BMU 40 Blood Monitoring Units Recalled for Electrical Safety Non-Compliance

    Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.

    Product
    Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0095-2021·2020-11-18

    Wolfgang Confectioners Recalls Hu Almond and Cashew Hunks Due to Mislabeling

    Wolfgang Confectioners is recalling Hu Almond Hunks and Hu Cashew Hunks because cashews were found in the almond product pouches.

    Product
    Hu Cashew Hunks, Hu Cashews + Vanilla Bean Chocolate Covered Hunks 4 oz., stand up pouch, 6 bags per case .
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0434-2021·2020-11-18

    Inpeco Aptio Automation System Recall for Potential Sample Dilution

    Inpeco S.A. is recalling 104 Aptio Automation Systems with Aliquoter Modules because a software error may cause samples to be diluted with water, leading to erroneous test results.

    Product
    Aptio Automation System with the Aliquoter Module (Inpeco P/N FLX-212) The FlexLab (aka Accelerator a3600 and Aptio Automation) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in…
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·20V716000·2020-11-18

    2021 Volkswagen Atlas and Select Models: Rear Camera Malfunction Risk

    Volkswagen is recalling certain 2021 Atlas and related models because the rear view camera may malfunction during startup, showing a black screen or frozen image, reducing visibility when reversing and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ARTEON, GOLF, JETTA, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0433-2021·2020-11-18

    Inpeco Accelerator a3600 Aliquoter Module Recall for Sample Dilution Risk

    Inpeco S.A. is recalling 136 Accelerator a3600 Automation Systems with Aliquoter Modules due to a software error that may dilute samples with water, leading to erroneous test results.

    Product
    Accelerator a3600 Automation System with the Aliquoter Module (Inpeco P/N FLX-212) The FlexLab (aka Accelerator a3600 and Aptio Automation) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0114-2021·2020-11-18

    Starwest Botanicals Recalls Organic Elderberry Tea Due to Salmonella Risk

    Starwest Botanicals is recalling specific lots of organic elderberry tea after a customer test detected Salmonella.

    Product
    Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia 1 lb. and 4 oz. Distributed in Mylar bags. 1 lb. UPC: 7 67963 07315 0; Item # 209290-01 4 oz. UPC 7 67963-10561-5; Item # 209290-04 Daily serving size; Pour 8-12 oz. of boiling water (212 degrees F) over 1 tsp…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V711000·2020-11-17

    Thor Motor Coach Motorhomes Electrical Fire Risk Battery Isolation Recall

    Thor Motor Coach is recalling certain 2020-2021 motorhomes. A faulty Battery Isolation Manager/Relay allows water into the engine compartment, creating electrical arcing and fire risk. Owners should contact TMC at 1-877-855-2867.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, DAYBREAK, FOUR WINDS, QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V708000·2020-11-17

    Altec Recalls AH150 and AH125 Aerial Devices Due to Valve Defect

    Altec is recalling 2006-2020 AH150 and AH125 aerial devices because an incorrect counterbalance valve may cause the boom to lower unexpectedly, increasing injury risk.

    Product
    ALTEC — ALTEC AH125, AH150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V712000·2020-11-17

    Volkswagen Atlas Vehicles Recalled for Steering Knuckle Damage

    Volkswagen is recalling certain 2021 Atlas and 2020-2021 Atlas Cross Sport vehicles with damaged steering knuckles that may fail during operation. A failed steering knuckle can cause loss of steering control, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V706000·2020-11-16

    2021 Motorhomes Recalled for Bed Lift Motor Failure and Collapse Risk

    REV Recreation Group is recalling certain 2021 motorhomes (Fleetwood and Holiday Rambler models) because the primary gear in the bed lift motor may fail, allowing the bed frame to drop and increase injury risk.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD NAVIGATOR, NAUTICA, ENDEAVOR, ARMADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-11152020-01·2020-11-15

    Tucson Tamale Wholesale Recalls Chicken and Pork Tamales Due to Plastic Contamination

    Tucson Tamale Wholesale Company LLC is recalling frozen chicken and pork tamales because they may contain hard plastic from diced tomatoes in puree.

    Product
    Tucson Tamale Wholesale Company LLC — FSIS Issues Public Health Alert for Chicken and Pork Tamales Containing FDA-Regulated Diced Tomatoes in Puree That Have Been Recalled Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide