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.

25276–25300 of 50443

  • HighFDA (Food)·F-1954-2019·2019-08-07

    Green Giant Fresh Ramen Soup Bowl Recalled for Listeria Risk

    Growers Express is recalling Green Giant Fresh Ramen Soup Bowls after a positive Listeria monocytogenes test result from a Massachusetts retail sample.

    Product
    Green Giant Fresh Ramen Soup Bowl; Butternut squash, Cauliflower, Carrots, Onions & Broccoli. Asian Inspired Seasoning and Roasted Edamame 7.4 oz.(209.8 g) plastic bag UPC:605806027864 ; Item number MXC183104 Perishable, Keep Refrigerated Distributed by Growers Marketing…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2113-2019·2019-08-07

    Burlington Medical Recalls Radiation Protection Vests Due to Inadequate Shielding

    Burlington Medical is recalling 22 radiation protection vests because the protective material may provide inadequate shielding against scatter radiation.

    Product
    Vest, Single Item, Product Number Vest, Part Numbers ECREVESTD, ECREVESTF, ECREVESTXLF, REVEST*M, REVESTB, REVESTC, SEVEST*F, SEVEST*M, SEVESTA, SEVESTB, SEVESTC, UEVESTB, UEVESTXLM Product Usage: Products are designed to protect healthcare workers against scatter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2130-2019·2019-08-07

    Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection

    Burlington Medical is recalling 23 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially increasing health risks for users.

    Product
    Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R, RETS3-R, RLTS3-R, RLTS3-SEP, RLTS3-T2T Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2086-2019·2019-08-07

    Teleflex Recalls Rusch EasyCath Kits Due to Sterility Concerns

    Teleflex Medical is recalling 3,700 Rusch EasyCath Kits because they may not be sterile. The kits were distributed nationwide to eight states.

    Product
    Rusch EasyCath Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2112-2019·2019-08-07

    Burlington Medical Recalls 310 Full Wrap Vests and Kilts for Radiation Protection Defects

    Burlington Medical is recalling 310 two-piece full wrap vests and kilts because the protective material may provide inadequate shielding against scatter radiation.

    Product
    2 pc Full Wrap Vest & Kilt, Product Number VK, Part Numbers ECREVKA, ECREVKB, ECREVKC, ECREVKXLM, ECSEVKA, ECSEVKB, ECSEVKC, ECSEVKXLM, REVK*F, REVK*M, REVKB, REVKC, REVKE, REVKXXLM, SEVK*F, SEVK*M, SEVKB, SEVKC, SEVKE, SEVKF, SEVKG, SEVKXLF, SEVKXXLM, UEVK*F, UEVK*M, UEVKXXLF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2099-2019·2019-08-07

    Inovo Single Luman Conserver Recalled for Potential Pressure Gauge Dislodgement

    Inovo, Inc. is recalling 690 Single Luman Conservers because the pressure gauge may dislodge from the mount, creating a leak.

    Product
    Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxygen from an oxygen tank and only deliver oxygen as the patient inhales, resulting in greater efficiency and cost saving ratios.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1957-2019·2019-08-07

    Growers Express Recalls Trader Joe's Butternut Squash Spirals for Listeria

    Growers Express is recalling Trader Joe's Butternut Squash Spirals after a positive Listeria monocytogenes test result was found in a random sample.

    Product
    Trader Joe's Butternut Squash Spirals 10.5 oz. (298 g). plastic bag UPC:623391 Item number BCN105106; Perishable, Keep Refrigerated
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-1955-2019·2019-08-07

    Growers Express Fresh Butternut Squash Recalled for Listeria Risk

    Growers Express is recalling fresh butternut squash due to a positive Listeria monocytogenes test result from a random sample.

    Product
    Growers Express Fresh Butternut Peeled; 10 lb. plastic bag No UPC: Food Service; Item number BNC103103 - sold at Native Maine sold in PA No UPC: Food Service, Item number BNC103102 - sold at Ruby Robinson (PFG) - ME. Perishable, Keep Refrigerated Distributed by Growers…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2119-2019·2019-08-07

    Burlington Medical Recalls Thyroid Collars Due to Inadequate Radiation Protection

    Burlington Medical is recalling 210 thyroid collars because the protective material may provide inadequate protection against scatter radiation, potentially exposing users to increased health risks.

    Product
    Thyroid Collar, Magnetic Closure, Product Number TS5, Part Numbers RBTS5-R, RBTS5-T2T, RLTS5-R, RLTS5-T2T, SLTS5-R Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1578-2019·2019-08-07

    ImprimisRx Recalls Subpotent Timolol-Latanoprost Ophthalmic Drops Nationwide

    ImprimisRx NJ is voluntarily recalling 405 bottles of Timolol-Latanoprost P-F ophthalmic drops because the medication was found to be subpotent.

    Product
    Timolol-Latanoprost P-F (0.5/0.005%) ophthalmic drops, packaged in 5mL bottles, Rx only, ImprimisRX NJ 1705 Route 46 West, Suite 4, Ledgewood, NJ 07852 (844) 446-6979
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2019·2019-08-07

    Burlington Medical Recalls Radiation Protection Kilts Due to Inadequate Shielding

    Burlington Medical is recalling 37 radiation protection kilts because the protective material may provide inadequate shielding against scatter radiation.

    Product
    Kilt, Single Item, Product Number Kilt, Part Numbers ECREKILTF, ECREKILTXLF, REKILTA, REKILTB, REKILTXLF, REKILTXLM, REKILT*M, SEKILTB, SEKILTC, SEKILT*F, SEKILT*M Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1946-2019·2019-08-07

    Sunnyside Farms Peach Yogurt Recalled for Coconut Allergen Contamination

    Super Store Industries is recalling Sunnyside Farms Peach Yogurt due to potential coconut contamination. The product was distributed in California.

    Product
    SUNNYSIDE FARMS PRESTIRRED PEACH YOGURT WITH OTHER NATURAL FLAVORS, 6 OZ (170g) CUP;99% Fat Free UPC# 7-17544-20293-6 Distributed by Super Store Industries, P.O. Box 549, Lathrop, Ca 95330 Filled at Plant 06-26
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·19V576000·2019-08-06

    Toyota Recalls 2019 RAV4 Models for Backup Camera Defect

    Toyota is recalling 2019 RAV4 and RAV4 Hybrid vehicles because a damaged electrical connector may prevent the backup camera from activating, increasing crash risk.

    Product
    TOYOTA — TOYOTA RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V575000·2019-08-05

    Ford Recalls 2020 Explorer and Lincoln Aviator for Parking Brake Cover Issue

    Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a missing parking brake cover or Factory Mode setting may allow the vehicle to roll away or hide gear selection.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V574000·2019-08-05

    Harley-Davidson Recalls Touring Motorcycles for Missing Rear Reflectors

    Harley-Davidson is recalling specific Touring and CVO Touring motorcycles because a luggage conversion kit removed rear red reflectors without providing replacements, reducing visibility.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRUSE, FLHTK, FLHTCUL, FLHTKSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V571000·2019-08-02

    Mercedes-Benz Recalls SL Models for Passenger Air Bag Seam Defect

    Mercedes-Benz is recalling certain 2018-2019 SL models because the front passenger air bag seam may tear during deployment, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SL 550, SL 450, AMG SL65, AMG SL63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2011-2019·2019-07-31

    Philips BrightView XCT Medical Device Recalled for Handcontroller Motion Defect

    Philips Medical Systems is recalling 427 BrightView XCT devices because a handcontroller issue may cause uncommanded motions or continued motion after buttons are released.

    Product
    BrightView XCT , Model Number 882482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1593-2019·2019-07-31

    Wegmans Assorted Whole Wheat Muffins Recalled for Potential Plastic Contamination

    Wegmans is recalling Assorted Whole Wheat Muffins because they may contain pieces of plastic. The recall affects products sold in several northeastern and mid-Atlantic states.

    Product
    Wegmans Assorted Whole Wheat Muffins, 4 Pack of Muffins; may contain a variety of flavors, which may include Carrot Apple Muffins, Sold in Square Plastic Clamshell with 4 wells for muffins UPC Codes: 77890-22745
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2060-2019·2019-07-31

    GE Healthcare Recalls MAC VU360 Electrocardiographs Due to Patient ID Errors

    GE Healthcare is recalling 369 MAC VU360 electrocardiographs because they may display incorrect patient IDs or demographics, potentially assigning ECG reports to the wrong patient.

    Product
    MAC VU360, Model Number 2030360-001, Electrocardiograph
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2026-2019·2019-07-31

    Siemens AXIOM Artis TC X-ray Generator Recall for Power Supply Issue

    Siemens is recalling one AXIOM Artis TC unit due to a power supply tolerance issue that may cause X-ray generation failure during procedures.

    Product
    AXIOM Artis TC, Model Number 7728350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2080-2019·2019-07-31

    Bard Nautilus Delta Port Kits Recalled for ECG Signal Loss

    Bard Peripheral Vascular is recalling specific Nautilus Delta Port Kits due to a risk of losing the intravascular ECG signal during placement procedures.

    Product
    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2039-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
    Category
    Medical Device
    Distribution
    Distributed nationwide