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.

29601–29625 of 50499

  • HighFDA (Devices)·Z-0989-2018·2018-03-21

    Alden Classic 55 Toric Contact Lenses Recalled for Sterility Issues

    Alden Optical is recalling Alden Classic 55 Toric Daily Wear Soft contact lenses because they lack sterility assurance. The recall affects units distributed in the US and Canada.

    Product
    Alden Classic 55 Toric Daily Wear Soft contact; Catalog Number: AOCLT55 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0968-2018·2018-03-21

    BD Vacutainer K2 EDTA Blood Collection Tubes Recalled for Additive Deficiency

    Becton Dickinson is recalling specific lots of BD Vacutainer K2 EDTA blood collection tubes because they may contain insufficient anticoagulant, potentially causing erroneous test results.

    Product
    BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematology determinations, immunohematology testing and blood donor screening.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18127·2018-03-20

    Briggs & Stratton Recalls Riding Mowers Due to Reverse Mow Malfunction

    Briggs & Stratton is recalling Snapper, Simplicity, and Massey Ferguson riding mowers because a malfunctioning switch may allow the mower to mow while reversing, posing a risk of injury.

    Product
    Snapper, Simplicity, and Massey Ferguson riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18731·2018-03-19

    Carrier Recalls Commercial Rooftop HVAC Units Due to Fire Hazard

    Carrier is recalling about 530 commercial rooftop HVAC units because a humidifier fan may fail to shut off, posing a fire hazard. No injuries have been reported.

    Product
    Carrier WeatherExpert commercial packaged rooftop HVAC units with humidimizer option
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V177000·2018-03-15

    Mercedes-Benz Recalls GLC Models for Retracting Rear Seat Belt Latch Plates

    Mercedes-Benz is recalling certain 2016-2018 GLC models because rear seat belt latch plates may retract into the interior paneling, preventing use.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC300, AMG GLC43, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18125·2018-03-15

    Louis Garneau Recalls Bicycle Helmets Due to Head Injury Risk

    Louis Garneau is recalling specific Course bicycle helmets because they do not meet federal impact safety standards, posing a risk of head injury.

    Product
    Bicycle helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V175000·2018-03-15

    Pagani Recalls 2017 Huayra Vehicles Due to Battery Software Defect

    Pagani is recalling 2017 Huayra Coupe BC and Roadster vehicles because battery management software may prevent the car from starting or idling, increasing crash risk.

    Product
    PAGANI — PAGANI HUAYRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18730·2018-03-15

    eheat Recalls Envi Wall Heaters Due to Overheating and Burn Hazard

    eheat is recalling about 35,000 Envi wall heaters sold in the U.S. and Canada due to a defect that can cause overheating, smoke, or melting, posing a burn hazard.

    Product
    Envi high-efficiency electric panel heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0909-2018·2018-03-14

    Roche cobas 6000 Modular Series System Warning Added to Prevent Operator Injury

    Roche Diagnostics is adding a warning to cobas 6000 and 8000 Modular Series Operator Manuals to prevent operator injury during maintenance.

    Product
    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Food)·F-0882-2018·2018-03-14

    Bob's Red Mill Recalls Buttermilk Pancake Mix for Undeclared Milk

    Bob's Red Mill is recalling 25 lb. bags of Buttermilk Pancake and Waffle Mix because the label failed to list milk as an ingredient.

    Product
    Buttermilk Pancake and Waffle Mix, Item number: 6170B25, packaged in 25 lbs. bulk kraft bag. The label is read in parts: "***BUTTERMILK PANCAKE & WAFFLE MIX***Net Wt 25 LB *** INGREDIENTS: Organic Whole Grain Buckwheat Flour, Organic Stone Ground Whole Wheat Pastry Flour…
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0922-2018·2018-03-14

    Abbott ARCHITECT c8000 Cuvette Segment Recall for False Test Results

    Abbott is recalling ARCHITECT c8000 Cuvette Segments because a detached post can cause falsely depressed patient results on c4000, c8000, and c16000 instruments.

    Product
    ARCHITECT c8000 Cuvette Segment, Part #01G46-01/01G06, a component to the ARCHITECT Clinical Chemistry system. There are 11 segments with each cuvette segment holding 15 cuvettes for a total of 165 cuvettes per reaction carousel. The firm name on the label is Abbott…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0903-2018·2018-03-14

    Synthes Reaming Rods Recalled for Potential Sterility Seal Defects

    Synthes (USA) Products LLC is recalling 1,144 sterile 2.5 mm Reaming Rods due to potential gaps in the package seal that may compromise sterility.

    Product
    2.5 mm Reaming Rod, Ball tip, 1150 mm, sterile, Part Number: 351.708S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0892-2018·2018-03-14

    Heartland Coca-Cola Recalls Sprite Zero Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Sprite Zero cans because sharp edges on the cans could cut consumers' mouths.

    Product
    Sprite Zero, Lemon-Lime Soda, Zero Calories, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0902-2018·2018-03-14

    Heartland Coca-Cola Recalls Sprite Cans With Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Sprite cans due to sharp edges that could cause cuts to consumers' mouths.

    Product
    Sprite, Lemon-Lime Soda, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0889-2018·2018-03-14

    Heartland Coca-Cola Recalls Pibb Zero Cans Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Pibb Zero soda cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Pibb Zero, Artificially Flavored Sugar Free Spicy Cherry Soda 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0903-2018·2018-03-14

    Heartland Coca-Cola Vanilla Zero Cans Recalled for Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling 766,271 cases of Coca-Cola Vanilla Zero 12 oz cans due to sharp edges that may cause mouth cuts.

    Product
    Coca-cola, Vanilla Zero, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0923-2018·2018-03-14

    Abbott Recalls ARCHITECT c16000 Cuvette Segments Due to Falsely Depressed Results

    Abbott Laboratories is recalling cuvette segments for the ARCHITECT Clinical Chemistry system because detached segment posts may cause falsely depressed patient test results.

    Product
    ARCHITECT c16000 Cuvette Segment, Part #09D32-05/ 03L77, a component to the ARCHITECT Clinical Chemistry system. There are 15 segments with each cuvette segment holding 11 cuvette pairs (22 cuvettes) for a total of 165 cuvettes pairs or a total of 330 cuvettes (22 cuvettes x 15…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0927-2018·2018-03-14

    Medtronic O-arm O2 Imaging System Recalled for Electrical Shock Risk

    Medtronic is recalling 449 O-arm O2 Imaging Systems because servicing internal components may cause an electrical short, posing a shock hazard to field service technicians.

    Product
    O-arm¿ O2 interventional fluoroscopic x-ray system; Catalog Number: B1-700-02000 The O-arm O2 Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients weighting 60 lbs or greater and having an abdominal thickness of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0906-2018·2018-03-14

    Dr Pepper Diet Cans Recalled Due to Sharp Edges

    Heartland Coca-Cola Bottling Company is recalling Dr Pepper Diet cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.

    Product
    Dr Pepper Diet, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of Dr Pepper Company, Plano, TX
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0846-2018·2018-03-14

    Mindray A-Series Anesthesia Delivery System Software Recall

    Mindray is recalling 2,875 A-Series anesthesia delivery systems due to a software issue that may apply incorrect settings or skip startup leak tests.

    Product
    A-Series A3/A5 Anesthesia Delivery System; Model Numbers: 0633F-01000-0X (A3) and 0631F-01000-0X (A5) Product Usage: The A-Series Anesthesia System is a device used to administer to a patient, continuously or intermittently, a general inhalation anesthetic, and to maintain a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0887-2018·2018-03-14

    Gilster-Mary Lee Recalls Puffed Rice Cereal Due to Undeclared Wheat Allergen

    Gilster-Mary Lee Corp. is recalling Food Club and Essential Choice Puffed Rice cereal because it was packaged with undeclared wheat, posing a risk to consumers with wheat allergies.

    Product
    Food Club, Essential Choice, Puffed Rice, Net Wt 6 Oz (170 g), UPC 36800 31852
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0844-2018·2018-03-14

    Toshiba Fluoroscopic X-Ray Systems Recalled for Ceiling Drive Bolt Loosening

    Toshiba American Medical Systems is recalling 29 INFX-8000V and INFINIX CF-I/BP PLUS systems because fastening bolts on the ceiling drive loosened, disabling operation.

    Product
    INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM
    Category
    Medical Device
    Distribution
    0 states