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.

21526–21550 of 50426

  • HighFDA (Food)·F-0163-2021·2020-12-16

    Pacific Coast Producers Recalls Tomato Paste Due to Metal Shavings

    Pacific Coast Producers is recalling 31,572 cases of 6-ounce tomato paste cans due to the presence of metal shavings. The product was distributed across the United States under multiple brand names.

    Product
    Tomato Paste in a 6 oz.(170g) metal can Cases size varies - 12, 24 or 28 count. Packaged under brand names of: Happy Harvest, Kroger, Signature Select, Food Club, Members Mark, Great Value, Essential Everyday, Summer is Inside, Harmons, Pastene, Avenue A.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0166-2021·2020-12-16

    Kroger HomeChef Buffalo Pretzel Chicken Breast Meal Kit Recalled for Listeria Risk

    The Kroger Co is recalling 1,080 HomeChef meal kits because a supplier ingredient was suspect for Listeria species. No illnesses have been reported.

    Product
    HomeChef meal kit: Buffalo Pretzel Chicken Breast with Roasted Cauliflower and Broccoli. 29 ounce.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0545-2021·2020-12-16

    Philips IntelliVue MP2 Patient Monitors Recalled for Speaker Failure

    Philips is recalling two IntelliVue MP2 patient monitors because speaker failures may prevent audible alarms, potentially delaying patient treatment.

    Product
    Philips IntelliVue MP2 Patient Monitors (865040) - Product Usage: intended for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment and during patient transport inside and outside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2021·2020-12-16

    TissueTech Recalls PROKERA Slim Corneal Bandages Due to Microbial Contamination

    TissueTech, Inc. is recalling 75 units of PROKERA Slim non-sterile biologic corneal bandages due to potential exposure to microbial contamination.

    Product
    PROKERA Slim, non-sterile - Product Usage: Biologic corneal bandage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0537-2021·2020-12-16

    Chromsystems MassChrom Amino Acid Analysis Plasma Control Level I Recalled

    Chromsystems Instruments & Chemicals GmbH is recalling MassChrom Amino Acid Analysis Plasma Control Level I kits because they do not meet stability criteria and may impact results.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level I, Order No. 0471 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0159-2021·2020-12-16

    Chef Myron's Premium Shoyu Sauce Recalled for Gluten-Free Mislabeling

    JMH International is recalling Chef Myron's Premium Shoyu Sauce because it contains wheat-derived gluten despite a gluten-free claim.

    Product
    Chef Myron's Premium Shoyu Sauce, 1 GAL (3.78 L), Item # 400023077, 2 bottles/case; 5 GAL (18.92 L), Item # 400023279, plastic pail
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21054·2020-12-16

    BRP Recalls Can-Am Off-Road Screw Jacks Due to Crush Hazard

    BRP is recalling Can-Am Off-Road screw jacks because they can collapse, posing a crush hazard that could cause severe injury or death.

    Product
    Can-Am® Off-Road screw jacks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0167-2021·2020-12-16

    Kroger HomeChef Meal Kit Recalled Due to Suspect Listeria Ingredient

    The Kroger Co is recalling HomeChef meal kits because a pretzel breading ingredient was suspect for Listeria species, though the result was not confirmed.

    Product
    HomeChef meal kit:Steak and Walnut-Green Onion Sauce with roasted potatoes and creamed spinach.
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0547-2021·2020-12-16

    Randox Rx Series Mg Magnesium Test Kits Recalled for Performance Failure

    Randox Laboratories is recalling four kits of the Rx Series Mg Magnesium test due to reduced linearity performance.

    Product
    Randox Rx Series Mg - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine Catalogue Number: MG8326
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0534-2021·2020-12-16

    Shimadzu Mobile X-Ray System Recalled for Improper Handle Bolts

    Shimadzu Medical Systems is recalling 115 Mobile X-Ray Systems because the adjustable handle may have improper bolts, posing a risk of harm to individuals around the device.

    Product
    Shimadzu Mobile X-Ray System, MobileDaRt Evolution (MX8 Version), with adjustable handle option, Made in Japan - Product Usage: The device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0555-2021·2020-12-16

    Shimadzu Trinias Digital Angiography System Recalled for Ceiling Arm Software Issue

    Shimadzu is recalling 23 Trinias Digital Angiography Systems because a software defect may cause the ceiling arm to move unexpectedly, posing a risk of collision or harm to patients and operators.

    Product
    Trinias, Digital Angiography System containing a MH-200, Ceiling Suspended C-arm Support - Product Usage: intended to be used for cardiac angiography, neurovascular angiography, abdominal angiography, peripheral angiography, rotational angiography, multi-purpose angiography and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0554-2021·2020-12-16

    Shimadzu Bransist Safire Digital Angiography System Recalled for Software Defect

    Shimadzu Medical Systems is recalling seven Bransist Safire Digital Angiography Systems because a software issue could cause the ceiling arm to move unexpectedly, posing a risk of collision or harm.

    Product
    Bransist Safire, Digital Angiography System containing a MS-200 Ceiling Suspended C-arm Support - Product Usage: designed to provide fluoroscopic images of the patient during diagnostic surgical and interventional angiography and cardiology procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0162-2021·2020-12-16

    Victoria Taylor Sicilian Seasoning Recalled for Undeclared Sesame

    Victoria Gourmet is recalling 1,080 jars of Victoria Taylor Sicilian Seasoning sold in Canada because the product contains undeclared sesame.

    Product
    Victoria Taylor Seasonings Sicilian Seasoning/Assaisonement Sicilien; Italian style seasoning blend; 2.5oz; packaged in a glass jar. Canadian product only.
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·20V784000·2020-12-16

    Aston Martin Recalls 2021 DBX Vehicles for Missing Headliner Foam

    Aston Martin is recalling 151 2021 DBX vehicles because they were built without required headliner foam blocks, increasing injury risk in crashes.

    Product
    ASTON MARTIN — ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V781000·2020-12-15

    Ducati Scrambler motorcycles recalled due to electrical short-circuit fire risk

    Certain 2018-2021 Ducati Scrambler 1100 motorcycles may experience an electrical short-circuit when the exhaust valve cable contacts the positive battery wire, increasing fire risk. Dealers will install a new cable guide and cable tie at no charge.

    Product
    DUCATI — DUCATI SCRAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V783000·2020-12-15

    AEV Ambulances Recalled for Potential LCD Display Malfunction

    Halcore is recalling specific 2020-2021 AEV ambulances because electrical spikes may cause the emergency lighting and HVAC control display to lock up or fail.

    Product
    AEV — AEV TYPE 1 F-SERIES AMBULANCE, TRAUMAHAWK, FREIGHTLINER M2 AMBULANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V779000·2020-12-15

    Rosenbauer Emergency Vehicles Recalled for LCD Display Lockup Defect

    Rosenbauer America is recalling specific emergency vehicles because LCD displays may lock up due to voltage spikes, potentially delaying emergency efforts.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, AVENGER, WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V775000·2020-12-11

    Mercedes-Benz Recalls 2020 AMG GT Vehicles for Headlight Aim Defect

    Mercedes-Benz is recalling 2020 AMG GT vehicles because headlights may be aimed too high, reducing visibility of oncoming traffic and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V777000·2020-12-11

    Altec Recalls 2020 Aerial Devices Due to Boom Valve Defect

    Altec is recalling 2020 AN67-E100 aerial devices because a shuttle cartridge was installed instead of a plug, risking unintended boom movement and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21713·2020-12-10

    Thermo Tents Recalls Mór Series Tents Due to Fire Hazard

    Thermo Tents is recalling Mór Series tents because they are incorrectly labeled as fire retardant, posing a fire hazard.

    Product
    Crua Tri, Crua Loj, and Crua Cottage tents in the Mór Series
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21712·2020-12-10

    Scentsy Recalls Electrical Oil Warmers Due to Fire Hazard

    Scentsy is recalling Luminary Jack and Bless This Home electrical oil warmers because corrosion of electrical components poses a fire hazard.

    Product
    Scentsy Luminary Jack Warmer and Scentsy Bless This Home Warmer
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V766000·2020-12-10

    Subaru Recalls 2020 Outback and Legacy for Rearview Display Issues

    Subaru is recalling 2020 Outback and Legacy vehicles because a software update may cause the rearview display to shut off intermittently, increasing crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21714·2020-12-10

    Homfa Cabinets Recalled Due to Tip-Over and Entrapment Hazards

    Homfa HPB-087 and HPB-106 cabinets are recalled because they can tip over or entrap children if not anchored to the wall.

    Product
    Homfa HPB-087 and HPB-106 Cabinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide