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.

43101–43125 of 50511

  • HighFDA (Devices)·Z-1893-2013·2013-08-14

    Meijer Wound Closure Adhesive Surgical Tape Strips Recalled for Sterility Concerns

    ASO, LLC is recalling Meijer Wound Closure Adhesive Surgical Tape Strips because the manufacturer could not confirm the product's sterility.

    Product
    Meijer Wound Closure Adhesive Surgical Tape Strips 30 strips 1/4 in. x 4 in. Sterile latex free UPC # 719283595973 Used to secure, close and support small cuts and wounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V361000·2013-08-14

    Recreation by Design Recalls 2013 Travel Trailers Due to Awning Motor Defect

    Recreation by Design is recalling 2013 Monte Carlo, Royal Travel, and North American travel trailers because a damaged awning motor may cause the awning to unfurl unexpectedly, increasing injury or crash risk.

    Product
    MONTE CARLO — MONTE CARLO, ROYAL TRAVEL, NORTH AMERICAN 44 SC, 44 SC FW, 39 SC, 35 SC FW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1923-2013·2013-08-14

    BD Vacutainer Luer Adapter Recalled for Potential Blood Leakage and Low Draw Volume

    Becton Dickinson is recalling BD Vacutainer Multiple Sample and Direct Draw Luer Adapters due to potential blood leakage and low draw volume.

    Product
    BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1895-2013·2013-08-14

    TopCare Wound Closure Adhesive Surgical Tape Strips Recalled for Sterility Concerns

    ASO, LLC is recalling TopCare Wound Closure Adhesive Surgical Tape Strips because the manufacturer cannot confirm the product's sterility.

    Product
    TopCare Wound Closure Adhesive Surgical Tape Strips 30 strips 1/4 in. x 4 in. Sterile latex free UPC # 036800165854 Used to secure, close and support small cuts and wounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0834-2013·2013-08-14

    Ventana Discovery Ultra Staining Systems Recalled for Waste Fluid Overflow Risk

    Ventana Medical Systems is recalling 54 Discovery Ultra automated staining systems because waste fluid drainage may become restricted, leading to overflow and potential fluid migration.

    Product
    VENTANA (a member of the Roche Group) DISCOVERY ULTRA; REF/MU 750-601; Research Use Only Product Usage: Research Use Only-The DISCOVERY ULTRA Advanced Staining System is intended to automatically stain histological or cytological specimens on microscope slides with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2013·2013-08-14

    ASO Recalls Wound Closure Tape Strips Due to Sterility Concerns

    ASO, LLC is recalling Discount Drug Mart wound closure adhesive tape strips because the company cannot confirm the product is sterile.

    Product
    Discount Drug Mart Wound Closure Adhesive Surgical Tape Strips 30 strips 1/4 in. x 4 in. Sterile latex free UPC # 093351120374 Used to secure, close and support small cuts and wounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2013·2013-08-14

    CVS Pharmacy Wound Closure Adhesive Surgical Tape Strips Recalled for Sterility Concerns

    ASO, LLC is recalling CVS Pharmacy Wound Closure Adhesive Surgical Tape Strips because the manufacturer cannot confirm the product's sterility.

    Product
    CVS Pharmacy Wound Closure Adhesive Surgical Tape Strips 30 strips 1/4 in. x 4 in. Sterile latex free UPC # 050428102909 item # 409170 Used to secure, close and support small cuts and wounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V359000·2013-08-13

    Pierce Recalls One 2008 Oshkosh Trailer Due to Fire Risk

    Pierce Manufacturing is recalling one 2008 Oshkosh AMAMTH-2 trailer because a wheelchair lift cable may cause a short circuit and fire.

    Product
    OSHKOSH — OSHKOSH AMAMTH-2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V349000·2013-08-13

    Volvo Trucks Recall 2011-2012 Models for Wiper Motor Failure

    Volvo Trucks North America is recalling 2011-2012 VAH, VHD, VNL, and VNM trucks because the windshield wiper motor may fail, increasing crash risk.

    Product
    VOLVO — VOLVO VHD, VNM, VAH, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13263·2013-08-13

    Husqvarna Recalls 2013 Off-Road Motorcycles Due to Throttle Cable Crash Hazard

    Husqvarna is recalling about 260 2013 closed-course and competition off-road motorcycles because a malfunctioning throttle cable can cause the rider to lose speed control, posing a crash hazard.

    Product
    Husqvarna closed course/competition off-road motorcycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V350000·2013-08-08

    OBS Recalls Four Motorhomes Due to Power Awning Motor Defect

    OBS is recalling four motorhomes because a design change in the power awning motor assembly may cause screws to shear, potentially allowing the awning to unfurl unexpectedly.

    Product
    ROYAL — ROYAL, OBS RTBGN, ADVENTURE III, CONCEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V357000·2013-08-08

    Outdoors RV Recalls 2013-2014 Trailers Due to Awning Motor Defect

    Outdoors RV is recalling specific 2013-2014 Creek Side, Timber Ridge, Wind River, and Black Stone trailers because the power awning motor screws may shear, causing the awning to unfurl unexpectedly.

    Product
    TIMBER RIDGE — TIMBER RIDGE, CREEK SIDE, BLACK STONE 270DBHS, 20FQ, 22RB, 23BHS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13262·2013-08-08

    Holgate Toys Recalls Wegmans Playmat Sets Due to Choking Hazard

    Holgate Toys is recalling Wegmans Playmat Sets because wooden vehicle wheels can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    Wegmans Playmat Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1847-2013·2013-08-07

    Hospira Symbiq Infusion System Recalled for Secondary Audio Signal Failure

    Hospira Inc. is recalling 2,791 Symbiq Infusion Systems because the secondary audio signal fails to activate. The devices were distributed across 22 US states.

    Product
    The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents, nutritionals, electrolytes, blood and blood products via parenteral, enteral, intravenous, intra-arterial, subcutaneous, epidural, or irrigation routes of administration.
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Food)·F-1755-2013·2013-08-07

    Fisher's New England Clam Chowder Recalled for Undeclared Allergens

    Fisher's Homestyle Salads LLC is recalling New England Clam Chowder because the packaging fails to list milk, corn, and specific shellfish allergens.

    Product
    Fisher's Homestyle Salads LLC***New England Clam Chowder*** packaged in 5 lb and 10 lb plastic containers.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Drugs)·D-831-2013·2013-08-07

    Baxter Recalls DIANEAL Low Calcium Peritoneal Dialysis Solution Due to Container Defect

    Baxter Healthcare is recalling 39,486 containers of DIANEAL Low Calcium with Dextrose peritoneal dialysis solution because defective containers may leak when the closure is removed.

    Product
    DIANEAL LOW CALCIUM WITH DEXTROSE — DIANEAL LOW CALCIUM WITH DEXTROSE (SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·13V347000·2013-08-07

    Chalet RV Recalls 2013-2014 Truck Campers and Travel Trailers for Awning Defect

    Chalet RV is recalling 2013-2014 truck campers and travel trailers because a design change in the power awning motor may cause screws to shear, risking injury or a crash.

    Product
    TAKENA — TAKENA, CHALET TRUCK CAMPERS 1865, TS116FB, 2265, 1860
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1848-2013·2013-08-07

    Siemens Luminos dRF Fluoroscopic X-Ray System Recalled for Software Error

    Siemens is recalling four Luminos dRF Fluoroscopic X-Ray systems due to a software error that may cause the table to tilt and collide with the floor.

    Product
    Siemens Luminos dRF Fluoroscopic X-Ray system Fluoroscopic X-Ray system
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1837-2013·2013-08-07

    Omnicycle Elite Medical Exercise Equipment Recalled for Firmware Anomaly

    Accelerated Care Plus is recalling 1,001 Omnicycle Elite units due to a firmware anomaly that may cause the equipment to operate at an incorrect speed in reverse mode.

    Product
    Omnicycle Elite; US Importer and Distributor: Accelerated Care Plus, Reno NV. Manufactured by Medica Medizintechnik GmbH, Hochdorf, Germany. The product is indicated for powered exercise equipment intended for medical purposes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V348000·2013-08-07

    Intech Recalls 2013 Custom Trailers Due to Awning Motor Defect

    Intech is recalling 2013 custom trailers because a design change in the power awning motor may cause screws to shear, potentially allowing the awning to unfurl unexpectedly.

    Product
    INTECH — INTECH CUSTOM TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13259·2013-08-07

    Toysmith Recalls Light-Up Frogs and Ducks Due to Choking Hazard

    Toysmith is recalling light-up toy frogs and ducks sold at Cost Plus World Market because a metal pin can detach, posing a choking hazard.

    Product
    Light-up toy frogs and ducks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1821-2013·2013-08-07

    Synthes Synapse SD Drill Guide Recalled for Incorrect Etching

    Synthes USA HQ, Inc. is recalling two Synapse SD Drill Guides with incorrect etching. The error could lead to the use of the wrong drill size during surgery.

    Product
    Synthes Synapse SD Drill Guide, Part Number SD389.477, Lot Number 6913900 Indicated for Hooks, Plate/Rods, Rods and Screws when intended to promote fusion of the cervical spine fusion of the cervical spine and occipitocervical junction (occiput-T3), the plate/rod, rod, hook…
    Category
    Medical Device
    Distribution
    1 state