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.

26301–26325 of 50460

  • HighNHTSA·19V206000·2019-03-18

    Keystone Recalls 2019 Dutchmen Trailers Due to Cooktop Burn Hazard

    Keystone RV is recalling 2019 Dutchmen Coleman and Aspen Trail trailers because the cooktop may cause excessive heat buildup and burns when the furnace is on.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN, ASPEN TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19083·2019-03-14

    O'Brien Performer Pro Combo Water Skis Recalled for Injury Hazard

    O'Brien Watersports is recalling Performer Pro Combo water skis because the bindings can detach during falls, causing the skis to break and injure users.

    Product
    Performer Pro Combo water skis
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V203000·2019-03-14

    Chrysler Recalls 2019 Models for Instrument Cluster Illumination Defect

    Chrysler is recalling 2019 Dodge Challenger, Charger, and Chrysler 300 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19081·2019-03-14

    Brush Art Recalls WIC Nutrition Plates Due to Fire Hazard

    Brush Art is recalling WIC nutrition plates because they contain aluminum and are incorrectly labeled as microwave-safe, posing a fire hazard.

    Product
    WIC nutrition plates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V202000·2019-03-14

    Forest River Recalls 2018-2019 Motorhomes and Buses for Reversed Camera Image

    Forest River is recalling 2018-2019 motorhomes, work trucks, and shuttle buses because backup camera images may display in reverse, increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER, COACHMEN ALLSTAR, BERKSHIRE, FREELANDER, ORION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1140-2019·2019-03-13

    Schwan's Big Daddy's Bold Cheese Pizza Recalled for Plastic Contamination

    Schwan's is recalling Big Daddy's Bold Cheese Pizza because it may contain plastic pieces. The product was distributed to institutional customers in 23 states.

    Product
    Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For Institutional Use. Cook Before Serving. Keep Frozen. Manufactured by: SPC Global Supply Chain, Inc. Marshall, MN 56258
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-1225-2019·2019-03-13

    Marketside Butternut Squash Cubes Recalled Due to Listeria Risk

    Southern Specialties, Inc. is recalling Marketside Butternut Squash Cubes because a food contact surface at a supplier facility tested positive for Listeria monocytogenes.

    Product
    Marketside BUTTERNUT SQUASH CUBES 16 OZ (1LB) 454g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0975-2019·2019-03-13

    Draegar Medical Systems Recalls Omega Patient Monitor Software

    Draegar Medical Systems is recalling Omega patient monitor software due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Omega Systems These devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians, Nurses, and Technicians, who will determine when use of the device is indicated, based upon their professional assessment of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0985-2019·2019-03-13

    Siemens Uroskop Omnia Max Fluoroscopic X-ray System Recall for Swivel Arm Defect

    Siemens is recalling 191 Uroskop Omnia Max fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1138-2019·2019-03-13

    Jansal Valley Dukkah Recalled Due to Glass Contamination

    Friendly Fruit Market is recalling Jansal Valley Dukkah because a customer found a piece of glass in the product.

    Product
    JANSAL VALLEY DUKKAH NET WT 2.5 oz. (71 G). The product is packaged in a circular tin can with a clear lid. UPC: 7 08152 31773 0.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1224-2019·2019-03-13

    Marketside Green Beans Recalled Due to Listeria Contamination Risk

    Southern Specialties, Inc. is recalling Marketside Green Beans because a supplier's food contact surface tested positive for Listeria monocytogenes.

    Product
    Marketside GREEN BEANS NET WT 12 OZ (340g) and Marketside GREEN BEANS NET WT 32 OZ (2 LB) 907g
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0984-2019·2019-03-13

    Siemens Uroskop Omnia Fluoroscopic X-ray System Recalled for Monitor Arm Defect

    Siemens is recalling six Uroskop Omnia fluoroscopic X-ray systems because the swivel arm holding the monitors may become dislodged from the carrying arm.

    Product
    Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop Omnia is a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0973-2019·2019-03-13

    Stryker Reprocessed Arthroscopic Shavers Recalled for Display and Function Errors

    Stryker is recalling 14,265 reprocessed arthroscopic shavers that may display incorrect settings or error messages, preventing proper use during surgery.

    Product
    Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1143-2019·2019-03-13

    Meijer Recalls Chocolate Mint Chip Cookies Due to Undeclared Soy

    Meijer is recalling specific lots of Ultimate Chocolate Mint Chip Cookies because they contain undeclared soy. The recall covers products sold in Meijer stores nationwide.

    Product
    Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic clamshell 12 count UPC 4125014563 20 count UPC 4125014564
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V198000·2019-03-13

    TCI Recalls 2015 and 2017 Transtech Buses with Wheelchair Lift Defect

    Transportation Collaborative is recalling 2015 and 2017 Transtech buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    TRANS TECH — TRANS TECH CST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0971-2019·2019-03-13

    Abbott Recalls Architect Magnesium Assay Due to Depressed Urine Results

    Abbott is recalling Architect Magnesium assays because urine tests may show falsely low results. The recall covers 24,995 units distributed in the US and four other countries.

    Product
    ARCHITECT MAGNESIUM, (a) REF 7D70-21, (b) 7D70-31 The Magnesium assay is used for the quantitation of magnesium in human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0974-2019·2019-03-13

    Draeger Infinity Delta Patient Monitors Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling Infinity Delta patient monitors due to cybersecurity vulnerabilities that may cause device reboots or loss of functionality.

    Product
    Infinity Delta Family patient monitors The Infinity Delta Series (Delta/Delta XL/Kappa) monitors are intended to be used on adult, pediatric, and neonatal populations, with the exception of the parameter Cardiac Output, ST Segment Analysis, and arrhythmia which are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19080·2019-03-13

    H-E-B Recalls Sauté Pans Due to Glass Lid Laceration Hazard

    H-E-B is recalling Kitchen & Table 5.5 qt. Sauté Pans because the glass lids can crack or shatter, posing a laceration hazard.

    Product
    Kitchen & Table 5.5 qt. Sauté Pan with glass lid
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0970-2019·2019-03-13

    Pentax C2 CryoBalloon Controller Recalled for Overpressure Detection Failure

    Pentax of America Inc is recalling 45 C2 CryoBalloon Controllers because the device fails to detect balloon overpressure during specific nitrous oxide applications, posing a risk of patient injury.

    Product
    C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is intended to be used as a cryosurgical tool in the field of general surgery, specifically for endoscopic application and the ablation of dysplastic Barrett s…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1145-2019·2019-03-13

    Concord Foods Recalls Salsa Seasoning Mix for Undeclared Milk Allergen

    Concord Foods is recalling Mild Salsa Seasoning Mix packets because they contain undeclared milk, a major food allergen.

    Product
    Concord Fresh Success Mild Salsa Seasoning Mix, Packaged in a NET WT 1.05 OZ (30g) packet, UPC: 0 4140900229 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1227-2019·2019-03-13

    Southern Specialties Recalls French Beans Due to Listeria Risk

    Southern Specialties, Inc. is recalling French Beans because a supplier's food contact surface tested positive for Listeria monocytogenes.

    Product
    FRENCH BEANS 5LBS and FRENCH BEANS 1 LB
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0983-2019·2019-03-13

    Maquet Cardiovascular Recalls AXIUS Blower Mister Due to CO2 Flow Issues

    Maquet Cardiovascular is recalling AXIUS Blower Mister devices because a potential lack of carbon dioxide flow may cause procedural delays during off-pump coronary artery bypass surgery.

    Product
    AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0981-2019·2019-03-13

    BD MAX Enteric Bacterial Panel Recalled for False Negative Results

    Becton Dickinson is recalling 1,583 BD MAX Enteric Bacterial Panel kits due to false negative results for specific bacterial targets.

    Product
    BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the BD MAX System Catalog Number: 442963 The BD MAX Enteric Bacterial Panel performed on the BD MAX System is an automated in vitro diagnostic test for the direct qualitative detection and differentiation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·027-2019·2019-03-12

    Carnivore Meat Company Recalls Beef and Pork Sausage Due to Undeclared Soy

    Carnivore Meat Company is recalling approximately 379 pounds of raw beef and pork sausage products because they contain undeclared soy, a known allergen.

    Product
    LSI Specialty Meats — Carnivore Meat Company, LLC Recalls Beef and Pork Sausage Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states