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.

43726–43750 of 50511

  • HighNHTSA·13E019000·2013-04-22

    Dometic Recalls Motor-Powered Awning Models Due to Injury Risk

    Dometic is recalling specific motor-powered awnings and service kits because improper installation can damage the motor, causing the awning to unfurl unexpectedly and increase the risk of injury or a crash.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V150000·2013-04-19

    Prevost Recalls Coach Buses Due to Incorrect Emergency Window Decals

    Prevost is recalling specific coach buses because emergency window decals omit a required step to open the windows, potentially increasing injury risk in a crash.

    Product
    PREVOST — PREVOST XLII-45 ENTERTAINER, XLII-45, H3-45 VIP, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V151000·2013-04-19

    Forest River Recalls 2013 Shasta Revere Trailers Due to Incorrect Tire Labels

    Forest River is recalling 173 model year 2013 Shasta Revere trailers because incorrect tire load and pressure information on labels may lead to overinflation and sudden tire failure.

    Product
    SHASTA REVERE — SHASTA REVERE SHT27DB, SHT30BH, SHT27BH, SHT27KS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1295-2013·2013-04-17

    NatureBox Umami Almonds Recalled for Undeclared Wheat Allergen

    NatureBox is recalling 802 units of Umami Almonds because the product may contain wheat, which is not listed in the ingredient statement.

    Product
    NatureBox brand Umami Almonds packed in branded stand-up pouches (whole tamari flavored almonds), Net wt. 4.3 oz. No UPC Codes on the product, Product is processed and packaged by NatureBox, San Carlos, CA; NOTE: Product label DOES declare that it is "Packed in a…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1071-2013·2013-04-17

    J T Posey Recalls Biothane Restraint Cuffs Due to Tensile Strength Defect

    J T Posey Company is voluntarily recalling 1,673 Biothane Restraint Cuffs because they failed to meet tensile strength specifications, posing a risk of disconnection.

    Product
    Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit a patient's movement to the extent necessary for treatment or protection of the patient or others.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1097-2013·2013-04-17

    Siemens Recalls Angiographic X-Ray Systems Due to Table Collision Risk

    Siemens is recalling 51 angiographic x-ray systems because a malfunction in the table vertical lift could cause a collision if obstructed by a solid object.

    Product
    Iconos R200 C20, Iconos R200 T20, Iconos R100, Iconos MD, Iconos RHD, Luminos RF Classic, Luminos Fusion or Luminos Select. Angiographic x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1065-2013·2013-04-17

    Arrow International Recalls FiberOptix Intra-Aortic Balloon Catheter Kits

    Arrow International is recalling 637 units of FiberOptix Intra-Aortic Balloon Catheter Kits due to a potential internal leak at the fill port.

    Product
    Arrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 40 cc; Product Number: IAB-05840-LWS. The IAB is utilized for intra-aortic balloon counter-pulsation therapy.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1305-2013·2013-04-17

    ShanTea Enlightened Mind Mate Kukicha Recalled for Salmonella Risk

    ShanTea LLC is recalling 111 cases of Enlightened Mind Mate/Kukicha tea due to potential Salmonella contamination. The product was distributed in 12 states.

    Product
    ShanTea Enlightened Mind Mate/Kukicha (UPC 794504284102) USDA Organic.
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1082-2013·2013-04-17

    Physio Control Recalls LIFEPAK Defibrillators Due to Battery Depletion Risk

    Physio Control is recalling LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators because they may experience early internal battery depletion.

    Product
    The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1085-2013·2013-04-17

    Medtronic Recalls Paradigm Insulin Pumps Due to Cap Detachment Risk

    Medtronic is recalling Paradigm insulin infusion pumps because a drive support cap may detach and allow water to damage internal electronics.

    Product
    Medtronic MiniMed Paradigm Insulin Infusion Pumps Model Numbers: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K, MMT-723, MMT-723K, MMT-554, and MMT-754. Product Usage: Paradigm insulin infusion pumps are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1079-2013·2013-04-17

    Thermo Fisher CO2 Incubators Recalled for Hinge Failure

    Thermo Fisher Scientific is recalling 15,567 CO2 incubators manufactured before mid-2009 because their coated metal hinges have reportedly failed in the field.

    Product
    CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542, 3543, 3584, 3585, 3598, and 3599. Product Usage: Incubators are designed to maintain an optimal environment for the incubation of tissue and cell samples.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1077-2013·2013-04-17

    Siemens Medical Solutions Recalls Elekta MOSAIQ Software Due to Safety Risk

    Siemens Medical Solutions is recalling Elekta MOSAIQ Oncology Information System software versions below 2.41 due to a potential safety risk identified by the manufacturer.

    Product
    ELEKTA MOSAIQ SW version below 2.41 Product Usage: The intended use of the SIEMENS branded ARTISTE and ONCOR family of linear accelerator systems is to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1309-2013·2013-04-17

    Red Eagle Flour Tortillas Recalled for Undeclared Wheat

    Red Eagle Enterprises is recalling flour tortillas because they contain undeclared wheat, a major food allergen.

    Product
    Large Cheese Crisp & Burrito Size, one dozen, net wt. 30 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1061-2013·2013-04-17

    Stryker Recalls Baseplate Impactor Extractor Instruments Due to Handle Detachment

    Stryker Howmedica Osteonics is recalling 871 Baseplate Impactor Extractor instruments because the handle may detach from the cam during surgery.

    Product
    Stryker Orthopaedics Baseplate Impactor Extractor TRIATHLON Instruments. Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430 USA A subsidiary of Stryker Corporation. Made in USA. Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZIEU…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1096-2013·2013-04-17

    GE Healthcare Recalls LOGIQ Ultrasound Systems Due to Potential Skin Burn Risk

    GE Healthcare is recalling LOGIQ S8 and S7 ultrasound systems equipped with the S4-10-D probe due to a potential safety issue that may cause skin burns.

    Product
    GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) and LOGIQ S7 (with software revisions R1.0.1, R1.0.2 and R1.0.3) diagnostic ultrasound system with the S4-10-D Ultrasound Probe. The device is intended for use in ultrasound evaluation.
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-1100-2013·2013-04-17

    GE Healthcare Recalls Discovery MR750w Systems Due to Image Flip Defect

    GE Healthcare is recalling 46 Discovery MR750w 3.0T MRI systems worldwide due to a potential image flip issue that may result in incorrect anatomical localization.

    Product
    GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, parametric maps, and/or spectra,dynamic images of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1310-2013·2013-04-17

    Red Eagle Flour Tortillas Recalled for Undeclared Wheat Allergen

    Red Eagle Enterprises is recalling flour tortillas because they contain undeclared wheat, posing a risk to consumers with wheat allergies.

    Product
    Lite Thin Tortillas, one dozen., net wt. 15 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1308-2013·2013-04-17

    Giant Eagle Cookies Recalled for Undeclared Soy Allergen

    Giant Eagle is recalling Lotsa Chocolate Chip Cookies because the labels fail to declare soy lecithin, a major allergen present in the product.

    Product
    Giant Eagle Lotsa Chocolate Chip Cookies
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-1311-2013·2013-04-17

    Red Eagle Flour Tortillas Recalled for Undeclared Wheat

    Red Eagle Enterprises is recalling flour tortillas because they contain undeclared wheat, a major food allergen.

    Product
    Small Flour Gorditas, one dozen, net wt. 24 oz
    Category
    Food
    Distribution
    1 state