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.

22076–22100 of 50429

  • HighNHTSA·20E073000·2020-10-02

    Dick's Sporting Goods Recalls Field & Stream Kayak Cradles

    Dick's Sporting Goods is recalling Field & Stream Kayak Cradles because kayaks may fall off while driving, increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V605000·2020-10-02

    2021 Motorhome Bunk Bed Motor May Fail, Causing Bunk to Fall

    The P2K Bunk Bed System motor in certain 2021 Coachmen Sportscoach and Forest River Georgetown motorhomes may fail, causing the bunk to fall while the vehicle is in motion. This increases the risk of injury or a crash.

    Product
    COACHMEN — COACHMEN, FOREST RIVER SPORTSCOACH, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V608000·2020-10-02

    Mercedes-Benz Recalls 2019 C 300 for Center Console Lock Defect

    Mercedes-Benz is recalling 2019 C 300 vehicles because the center console lock may not function properly, increasing injury risk in rear-end crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V604000·2020-10-02

    Aston Martin Recalls Vehicles Due to Loose Front Seat Air Bag Fasteners

    Aston Martin is recalling specific 2017-2020 models because front seat air bag fasteners may not be tightened correctly, increasing injury risk.

    Product
    ASTON MARTIN — ASTON MARTIN VANTAGE, DB11, DBS SUPERLEGGERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V598000·2020-09-30

    BMW 2020-2021 Rearview Camera Software Obscures Rear View Image

    BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.

    Product
    BMW — BMW 530I, X3, X4, M550I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2985-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1346, Sterile EO, Rx Only, CE, UDI: 8022057015228 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3000-2020·2020-09-30

    ArthroCare Recalls SmartStitch Connectors Due to Manufacturing Error

    ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.

    Product
    Smith&Nephew SmartStitch PerfectPasser Connector, REF # OM-8010, Rx Only, CE 0123, UDI: 00817470006971
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2984-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1345, Sterile EO, Rx Only, CE, UDI: 8022057015204 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2989-2020·2020-09-30

    Wright Medical Recalls Evolve Stem Implants Due to Sterility Assurance Issues

    Wright Medical Technology is recalling 16 Evolve Stem 8.5mm implants because they lack sterility assurance. The recall covers units distributed in the US and several international countries.

    Product
    EVOLVE STEM 8.5MM Model # 496S085
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Drugs)·D-1620-2020·2020-09-30

    AJR Trading Recalls Bio AAA Alcohol Gel Due to Methanol Presence

    AJR Trading LLC is recalling 2,000 bottles of Bio AAA Alcohol Gel because methanol was found in other lots from the same facility.

    Product
    bio aaa Alcohol en Gel Antibacterial, Alcohol al 70% Cont. Neto 480 ml bottle, Hecho en Mexico por: AAA Cosmetica S.A. DE C.V. Recursos Hidraulicos No. 1 Secc. A, Col La Loma Zona Industrial, Tlalnepantla de Baz C.P. 54060 Edo. Mexico. UPC 7 502272 12108 5
    Category
    Drug
    Distribution
    1 state
  • HighNHTSA·20V601000·2020-09-30

    BMW recalls vehicles due to debris in hybrid battery cells

    BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.

    Product
    BMW — BMW, MINI 745LE, X5, 530E, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1542-2020·2020-09-30

    Gilster-Mary Lee Recalls Light Microwave Popcorn Due to Foreign Matter

    Gilster-Mary Lee Corp. is recalling specific lots of Full Circle and Nature's Promise light microwave popcorn because tempered glass pieces were found in the product.

    Product
    Light microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Light Butter, 3-2.9 oz (82 g) bags, Net Wt. 8.7 oz (247 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40610 2) Nature's Promise, Microwave Popcorn…
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1535-2020·2020-09-30

    Freshouse Produce Recalls Lemons Due to Listeria Monocytogenes

    Freshouse Produce is recalling 2 lb mesh bags of lemons sold as Fresh from the Start and Wegmans brands due to positive environmental sampling for Listeria monocytogenes.

    Product
    Lemons, 2lb mesh bag sold under the brand names of Fresh from the Start, UPC 33383 14020 & Wegmans, UPC 77890 15917
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-3012-2020·2020-09-30

    Irvine Biomedical Recalls Steerable Diagnostic Catheters Due to Labeling Error

    Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.

    Product
    Inquiry Steerable Diagnostic Catheter, REF: IBI-87002 - Product Usage: INDICATIONS FOR USE The Inquiry fixed curve and steerable electrophysiology catheters are used for electrogram recording and cardiac stimulation during diagnostic electrophysiology studies. The catheters are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1537-2020·2020-09-30

    Freshouse Produce Recalls Wegmans Valencia Oranges Due to Listeria Risk

    Freshouse Produce is recalling Wegmans Valencia Oranges after environmental sampling tested positive for Listeria monocytogenes. The product was distributed to wholesalers in Maryland and retailers in North Carolina, Pennsylvania, South Carolina, and Virginia.

    Product
    Wegmans Valencia Oranges, 4lb mesh bag, UPC 77890 52363
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-3013-2020·2020-09-30

    Medline Recalls Central Line Dressing Change Trays Due to Seal Defects

    Medline Industries is recalling Central Line Dressing Change Trays because incomplete seals may compromise sterility. The recall affects kits distributed in Minnesota and Texas.

    Product
    Central Line Dressing Change Tray
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2986-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.

    Product
    Perceval Single Use Accessory Kit, Size S, REF: ICV1349, Sterile EO, Rx Only, CE, UDI: 8022057015211 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1538-2020·2020-09-30

    Fresh from the Start Red B Potatoes Recalled for Listeria

    Freshouse Produce is recalling 8,262 bags of Fresh from the Start Red B Potatoes due to positive environmental sampling for Listeria monocytogenes.

    Product
    Fresh from the Start Red B Potatoes, 3lb mesh bag, UPC 33383 51003
    Category
    Food
    Distribution
    5 states
  • HighCPSC·20194·2020-09-30

    Petzl Recalls Low-Stretch Kernmantle Ropes Due to Fall and Injury Hazard

    Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.

    Product
    Low-Stretch Kernmantle Ropes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1541-2020·2020-09-30

    Gilster-Mary Lee Recalls Microwave Popcorn Due to Glass Contamination

    Gilster-Mary Lee Corp. is recalling Cadia and Lidl microwave popcorn because tempered glass fragments were found in the product.

    Product
    Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9 oz (281 g) 3-3.3 oz (94 g) bags, KeHDistributors LLC, Naperville, IL, UPC 15369-01288 2) Lidl, Naturally Flavored Butter Microwave Popcorn, 3-3.3 oz (94g)…
    Category
    Food
    Distribution
    21 states