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.

27326–27350 of 50462

  • HighFDA (Food)·F-0026-2019·2018-10-17

    Sarap Asian Fusion Recalls Ube Cookies & Cream for Undeclared Allergens

    Sarap Asian Fusion is recalling Ube Cookies & Cream because the product contains undeclared wheat, soy lecithin, and milk.

    Product
    Ube Cookies & Cream (cookies); A Sarap Asian Fusion Product; NET WT. 65 G/Cookie; Contains: Flour, eggs, Baking Soda, Baking Powder, Milk Powder, White Sugar, Brown Sugar, Salt, Butter, Ube, Vanilla extract, cookies & cream chocolate. MFG at 12042 West St. Garden Grove…
    Category
    Food
    Distribution
    44 states
  • HighFDA (Food)·F-0022-2019·2018-10-17

    Whole Foods Recalls 365 Everyday Value White Corn Chips for Undeclared Milk

    Whole Foods Market is recalling 365 Everyday Value White Corn Chips because they may contain undeclared milk. The affected products were distributed nationwide in the US and Canada.

    Product
    365 Everyday Value Brand White Corn Chips, Salted NET WT 20 oz. (1 LB 4 OZ) 567 g packaged in a plastic bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0091-2019·2018-10-17

    Durex Synthetic Polyisoprene Condoms Recalled for Burst Pressure Concerns

    Reckitt Benckiser LLC is recalling Durex Synthetic polyisoprene condoms in New York due to insufficient data ensuring they meet internal burst pressure specifications at the end of their 5-year shelf life.

    Product
    Polyisoprene condomns Product Usage: The Durex Synthetic polyisoprene male condom is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted disease).
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0080-2019·2018-10-17

    Ortho-Clinical Diagnostics Recalls VITROS 5600 Integrated Systems

    Ortho-Clinical Diagnostics is recalling refurbished VITROS 5600 Integrated Systems because they may dispense insufficient sample volumes without suppressing potentially incorrect results.

    Product
    VITROS 5600 Integrated System- (Refurbished). For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, Catalog Number: 6802915
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2019·2018-10-17

    Widex BABY Hearing Aids Recalled for Non-Tamper-Resistant Battery Drawers

    Widex A/S is recalling two BABY440 hearing aids because they were fitted with non-tamper-resistant battery drawers. The devices were distributed in Georgia and New York.

    Product
    Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is intended for, but not limited to, babies (0 to 3 years of age) to be used as air conduction amplification devices in everyday listening environments.
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·18V730000·2018-10-16

    Yamaha Recalls SR400 Motorcycles Due to Engine Oil Leak Risk

    Yamaha is recalling 2015-2018 SR400 motorcycles because an engine oil line nut may be loose, causing oil to leak onto the rear tire and increasing crash risk.

    Product
    YAMAHA — YAMAHA SR400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19010·2018-10-16

    Gold Recalls Eddie Bauer Infant Carriers Due to Fall Hazard

    Gold Inc. is recalling Eddie Bauer fabric infant carriers because buckles can break, posing a fall hazard to children. No injuries have been reported.

    Product
    Eddie Bauer fabric infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V722000·2018-10-15

    Forest River Recalls School Buses Due to Seat Foam Impact Defect

    Forest River is recalling certain Starcraft and StarTrans school buses because the seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, STARTRANS QUEST, PRODIGY, SENATOR II, QUEST XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V726000·2018-10-15

    Keystone Recalls 2019 Crossroads Fifth Wheels Due to Awning Switch Defect

    Keystone is recalling 2019 Crossroads Cruiser and Volante fifth wheels because defective awning switches may allow the awning to unroll while the vehicle is moving.

    Product
    CROSSROADS — CROSSROADS VOLANTE, CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V724000·2018-10-15

    Mercedes-Benz Recalls 2018 AMG GT Models for Air Bag Software Issue

    Mercedes-Benz is recalling 2018 AMG GT and AMG GT C Cabrio vehicles because a software error may cause both stages of the frontal air bags to deploy in a low-speed crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT, AMG GT C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V718000·2018-10-12

    Riverside Dream Trailer Recall for Awning Deployment Risk

    Riverside is recalling one 2018 Dream trailer because the awning may deploy while moving, increasing crash risk. Dealers will replace the awning controller free of charge.

    Product
    RIVERSIDE — RIVERSIDE DREAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V712000·2018-10-11

    Erwin Hymer Recalls 2018-2019 Motorhomes Due to Generator Overcharging

    Erwin Hymer is recalling 172 motorhomes because the generator may overcharge auxiliary batteries, potentially causing acid spills if non-sealed batteries are used.

    Product
    ROADTREK — ROADTREK, HYMER, CARADO SIMPLICITY SRT, AKTIV 2.0, AKTIV, BANFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3358-2018·2018-10-10

    B. Braun Medical Recalls CE18TKDP Catheter Connectors Due to Leakage

    B. Braun Medical is recalling CE18TKDP catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18TKDP CONT EPID/DURAPREP, Material Number 332215 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3373-2018·2018-10-10

    B. Braun Medical Recalls Epidural Catheter Connectors Due to Leakage

    B. Braun Medical is recalling 1,760 CE18TOD epidural tray connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CE18TOD CONT EPIDURAL TRAY LF, Material Number 332236 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3330-2018·2018-10-10

    B. Braun Medical Recalls 17GA Safety Tuohy Needle Trays

    B. Braun Medical is recalling 17GA Safety Tuohy Needle Trays because the catheter connectors may not stay closed, leading to leakage or disconnection.

    Product
    CE17TKFCY 17GA SAFETY TUOHY NEEDLE TRAY, Material Number 332075 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3327-2018·2018-10-10

    B. Braun Medical Recalls Catheter Connectors Due to Leakage and Disconnection

    B. Braun Medical is recalling 430 units of CONT STIM BASIC KIT W/4 IN INSUL TUOHY catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    CONT STIM BASIC KIT W/4 IN INSUL TUOHY, Material Number 331758 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3400-2018·2018-10-10

    B. Braun Medical Recalls EC20CST 20G Soft Tip Catheter Connectors

    B. Braun Medical is recalling EC20CST 20G Soft Tip Catheter Connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    EC20CST 20G CLSD SOFT TIP CATH, Material Number 333521 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0011-2019·2018-10-10

    Ellex iScience Recalls Canaloplasty Microcatheter Kits Due to Sterility Failure

    Ellex iScience is recalling 90 units of the iTRACK 250A Canaloplasty Microcatheter Kit because a sterility failure was found in one unit of the lot.

    Product
    ellex I.Science iTRACK 250A, Canaloplasty Microcatheter Kit, for single use, REF iT-250A, Rx. The firm name on the label is Ellex iScience, Inc., Fremont, CA. Used in ophthalmic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3402-2018·2018-10-10

    B. Braun Medical Recalls EC20C Catheter Connectors Due to Leakage

    B. Braun Medical is recalling EC20C catheter connectors because they may not stay closed, leading to leakage or disconnection.

    Product
    EC20C 20G X 100CM CATH CLOSED, Material Number 333540 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with…
    Category
    Medical Device
    Distribution
    Distributed nationwide