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.

25576–25600 of 50447

  • HighCPSC·19141·2019-06-21

    Honeywell Recalls Photoelectric Smoke Sensors for Fire Alarm Failure

    Honeywell is recalling about 22,000 photoelectric smoke sensors sold with fire alarm systems because they may fail to alert occupants of a fire.

    Product
    "-IV" Intelligent photoelectric smoke sensors sold with fire alarm systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V487000·2019-06-21

    Charles Machine Recalls Ditch Witch Trailers Due to Brake Terminal Defect

    Charles Machine is recalling 2018-2019 Ditch Witch trailers because improperly crimped brake wire terminals may cause the brakes to fail, increasing crash risk.

    Product
    CHARLES MACHINE — CHARLES MACHINE DITCH WITCH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19139·2019-06-20

    Hunter Brunswick Ceiling Fans Recalled Due to Electric Shock Hazard

    Hunter Fan Company is recalling Brunswick ceiling fans because damaged light kit wires pose an electric shock hazard. No injuries have been reported.

    Product
    Hunter Brunswick three and four light ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1752-2019·2019-06-19

    GE Healthcare Recalls Proteus XR/a Radiographic Systems Due to Monitor Fall Risk

    GE Healthcare is recalling 825 Proteus XR/a radiographic systems because a monitor fell off its wall mount due to product aging.

    Product
    Proteus XR/a The Proteus XR/a radiographic system offers the flexibility to choose a configuration based upon your specific requirements. The system provides exceptional image quality, high frequency X-ray generation, easy patient positioning, intuitive operator control and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1755-2019·2019-06-19

    GE Healthcare Recalls Silhouette VR Systems Due to Monitor Mount Failure

    GE Healthcare is recalling 825 Silhouette VR systems because a CRT monitor fell off its wall mount due to product aging.

    Product
    Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-saving design.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1352-2019·2019-06-19

    Torrent Pharma Recalls Banophen Oral Solution Due to Bacterial Contamination Risk

    Torrent Pharma Inc is recalling Banophen Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.

    Product
    Banophen Oral Solution, Sugar Free, Alcohol Free, Cherry Flavor, (Diphenhydramine HCl, USP) Each teaspoonful contains diphenhydramine hydrochloride, USP 12.5 mg, a) 4 Fl. oz. (118 mL) bottle, NDC: 0904-1228-00, b) One Pint (473 mL) bottle, NDC: 0904-5174-16, Distributed by Major…
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Food)·F-1457-2019·2019-06-19

    Park Street Deli Hummus Recalled for Undeclared Peanut Butter

    Del Monte Fresh Produce is recalling Park Street Deli Classic Hummus with Carrots & Celery due to undeclared peanut butter.

    Product
    Park Street Deli, Hummus and Veggies, Classic Hummus, Carrots & Celery NET WT 5 OZ (142g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1775-2019·2019-06-19

    Conformis iTotal Hip Replacement System Recalled for Dimensional Discrepancy

    Conformis, Inc. is recalling 128 iTotal Hip Replacement System stems due to a 3mm discrepancy between approved and manufactured neck/head lengths.

    Product
    Conformis iTotal Hip Replacement System: HBS-033-00xx-010101, (HIP-PATIENT SPECIFIC STEM LEFT)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1779-2019·2019-06-19

    Skytron Integrity 270 Steam Sterilizer Recalled for Weld Fatigue

    Skytron is recalling five Integrity 270 Steam Sterilizers because the weld attaching the air heater assembly has shown signs of fatigue or failure.

    Product
    Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam Product Usage: The SKYTRON Integrity 270 Steam Sterilizer for use in health care facilities. The Integrity Sterilizer incorporates high-pressure steam to sterilize nonporous or porous items and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1447-2019·2019-06-19

    Izzio Artisan Bakery 100% Rye Bread Recalled for Undeclared Wheat

    Izzio Artisan Bakery is recalling 100% Rye Bread because it may contain undeclared wheat. The product was distributed nationwide.

    Product
    Izzio Artisan Bakery 100% Rye Bread, Net Weight: 9 oz ; 8 slices per package, Flow Wrap Package. Frozen. Item #3301, Case UPC #657082033015, Unit UPC #657082033015
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V473000·2019-06-19

    Audi Recalls 2019 Q5 and SQ5 Models for Air Bag Defect

    Volkswagen Group of America is recalling 2019 Audi Q5 and SQ5 vehicles because a defective instrument panel carrier may damage the passenger air bag during a crash.

    Product
    AUDI — AUDI Q5, SQ5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1753-2019·2019-06-19

    GE Healthcare Recalls Prestilix 1600X Digital Radiology Systems

    GE Healthcare is recalling 825 Prestilix 1600X digital radiology systems because a monitor fell off its wall mount due to product aging.

    Product
    Prestilix 1600X Prestilix system is a fully integrated remote controlled digital radiology system. It is designed for all general radiology applications with or without contract injection and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2019·2019-06-19

    Medtronic InterStim System Recall for Unexpected Stimulation Increase

    Medtronic is recalling InterStim System kits due to a potential for unexpected stimulation increases during programming with the A10 Clinician Application.

    Product
    InterStim(TM) System, Model Numbers: a) TH90G01 b) TH90GFA c) TH90G02 d) TH90G03 Product Usage: The Medtronic Model A510 Clinician application (app) is intended for use with the HH90 Handset and TM90 Communicator to program, adjust, and troubleshoot the Medtronic Models…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1778-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling 40 Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86682003 Product Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1452-2019·2019-06-19

    Meiji Chocolate Macadamia Bars Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Macadamia bars because they lack English labels for nutrition facts, ingredients, and allergens.

    Product
    CHOCOLATE MACADAMIA MEIJI, 2.25 oz. Item number 69920 UPC 074410699208 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1777-2019·2019-06-19

    Getinge 86-Series Medical Washer-Disinfector Recalled for Potential Hose Collapse

    Maquet Cardiovascular is recalling four Getinge 86-Series Medical Washer-Disinfector units because the inlet pump hose may collapse, potentially preventing proper cleaning of medical instruments.

    Product
    Getinge 86-Series-Medical Washer-Disinfector Part Number: S-86662003 Product Usage: Usage: The Getinge 86 Series Medical Washer-Disinfector is designed for use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia sets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1780-2019·2019-06-19

    Cook Inc. Recalls Neff Percutaneous Access Sets Due to Sterility Concerns

    Cook Inc. is recalling 97 Neff Percutaneous Access Sets because they may have been manufactured without a bottom seal, compromising sterility. No US distribution occurred.

    Product
    Neff Percutaneous Access Set, Catalog Number NPAS-100-RH-NT
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1781-2019·2019-06-19

    GE Centricity PACS-IW Recall for Potential Missing Image Series

    GE Healthcare is recalling 620 units of Centricity PACS-IW software because image series may be missing from exams without a warning.

    Product
    GE Centricity PACS-IW versions 3.6.0 through 3.7.3.9 SP1, SP2, SP3 and 3.7.3 SPa10, Model Numbers: a) 2052831-00x b) 2050578-0xx c) 2090228-002 d) 2052782-00x
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1769-2019·2019-06-19

    Terumo Electronic Patient Gas System Recalled for Control Slider Failure

    Terumo is recalling 72 Electronic Patient Gas Systems used in cardio-pulmonary bypass because a fault disables control sliders, forcing use of local knobs.

    Product
    Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI 00886799000588. Used in cardio-pulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E041000·2019-06-19

    Gillig Recalls Transpec T287X Series Glass Roof Hatches for Shattering Risk

    Gillig LLC is recalling Transpec T287X Series glass roof hatches sold as aftermarket parts because temperature and vibration stresses may cause the tempered glass to shatter, potentially injuring passengers.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1454-2019·2019-06-19

    Meiji Chocolate Wheat Snack Recalled for Missing English Allergen Labels

    Wismettac Asian Foods is recalling Meiji Chocolate Takenoko no Sato bars because they lack English labels for ingredients and allergens, including milk, soy, egg, and tree nuts.

    Product
    CHOCOLATE TAKENOKO NO SATO MEIJI (Chocolate wheat snack, 2.46 oz. Item number 65880 UPC 074410658809 - only on those bars with English labeling. Distributed by Wismettac Asian Foods, Inc.
    Category
    Food
    Distribution
    6 states
  • HighNHTSA·19V474000·2019-06-19

    Audi Recalls Vehicles Due to Passenger Air Bag Deactivation Risk

    Audi is recalling specific 2015-2019 models because an electrical issue may cause the passenger air bag to deactivate, increasing injury risk in a crash.

    Product
    AUDI — AUDI A3 CABRIOLET, RS 3, A3 SPORTBACK E-TRON, S3
    Category
    Vehicle
    Distribution
    Distributed nationwide