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.

14326–14350 of 53090

  • HighNHTSA·23V102000·2023-02-20

    2022-2023 Jayco and Entegra Recreational Vehicles Recalled for Missing Weight Labels

    Jayco is recalling certain 2022-2023 recreational vehicles because certification labels are missing the rear Gross Axle Weight Rating. This missing information could lead to overloading and increase crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA GREYHAWK PRESTIGE, ACCOLADE, ACCOLADE XL, ESTEEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V106000·2023-02-20

    2022-2023 Polaris Slingshot Motorcycles Recalled for Faulty Alternator

    Certain 2022-2023 Polaris Slingshot motorcycles are recalled because the alternator may have been improperly heat-treated during manufacturing. The defect could cause the alternator to crack and separate during operation, increasing fire risk.

    Product
    POLARIS — POLARIS SLINGSHOT S, SLINGSHOT SL, SLINGSHOT SLR, SLINGSHOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V101000·2023-02-17

    2022 Mercedes-Benz Sprinter Airbag Non-Deployment Risk from Wiring Defect

    Certain 2022 Mercedes-Benz Sprinter vehicles with adjustable front swivel-seats have wiring harnesses that may be incorrectly installed, causing side airbags to fail deployment in a crash and increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V099000·2023-02-17

    2023 BMW vehicles recalled for unintended power window and sunroof closure

    BMW is recalling 2023 and some 2022 model-year vehicles for a software defect allowing power windows and sunroofs to close without the digital key present, posing a risk of injury to occupants.

    Product
    BMW — BMW Z4, M850I, 840I, 230I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V097000·2023-02-17

    Vehicle recall: Mercedes-Benz G550 and AMG G63 front axle wiring chafe

    2019–2021 Mercedes-Benz G550 and AMG G63 models may lose anti-lock brakes and stability control due to front axle wiring harness chafing against the oil cooler, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63, G 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V096000·2023-02-17

    Pierce Aerial Trucks Recalled for Basket Handrail Detachment Risk

    Pierce is recalling 2018-2023 Arrow XT, Enforcer, Velocity, and Impel 110-foot aerial trucks because the basket handrail may detach when the platform is extended.

    Product
    PIERCE — PIERCE VELOCITY, ENFORCER, ARROW XT, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23125·2023-02-16

    KLIM Backcountry Probes A300 Recalled Due to Failure Risk

    KLIM Backcountry Probes A300 can fail to operate when deployed to locate avalanche victims, posing a risk of severe injury or death. Consumers should stop using the product immediately and contact KLIM for a full refund.

    Product
    KLIM Backcountry Probes A300
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V089000·2023-02-16

    Dennis Eagle Proview Recalled for Dim Front Turn Signal Lights

    Dennis Eagle is recalling 2020-2023 Proview vehicles because front turn signal lights may not flash brightly enough, increasing crash risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V095000·2023-02-16

    Electra Meccanica Solo G2 and G3 recalled for sudden loss of drive power

    Electra Meccanica is recalling 2019-2023 Solo vehicles due to a defect in the motor controller or battery controller that can cause sudden loss of drive power, increasing crash risk. Owners are being notified and eligible for vehicle repurchase.

    Product
    ELECTRAMECCANICA — ELECTRAMECCANICA SOLO G3, SOLO G2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V093000·2023-02-16

    2020 Nissan Rogue Ignition Key May Collapse While Driving

    Nissan is recalling certain 2020 Rogues and Rogue Sports due to a faulty ignition key that may collapse while driving. The collapse could shut off the engine and prevent airbag deployment in a crash.

    Product
    NISSAN — NISSAN ROGUE, ROGUE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23122·2023-02-16

    Hatley USA Children's Pajamas and Headbands Recalled

    Hatley USA is recalling about 7,640 children's pajamas and about 300 headbands. The pajamas fail to meet federal flammability standards and pose a burn hazard; the headbands contain excess lead that is toxic if ingested.

    Product
    Children's pajamas and headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23120·2023-02-16

    Wicked Lights ScanPro Night Hunting Headlamps Recalled for Burn Hazard

    AllPredatorCalls.com is recalling approximately 12,000 Wicked Lights ScanPro night hunting headlamps because a wire short can cause the wire to heat up and melt, posing a burn hazard. The company has received 14 reports of wire heating and melting, including two burn injuries.

    Product
    Wicked Lights ScanPro Night Hunting Headlamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23121·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    The Oaks Apparel Company is recalling about 320 children's nightgowns that fail to meet federal flammability standards for sleepwear, posing a burn injury risk. Consumers should stop using them immediately.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V092000·2023-02-16

    2023 Honda CR-V Passenger Seat Back Frame Welding Defect

    Honda is recalling 2023 CR-V vehicles due to improper welding of the front passenger seat back frame, which may fail in a crash and increase injury risk.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23127·2023-02-16

    Kids Preferred Disney Character Figurines Recalled for Choking Hazard

    Kids Preferred is recalling soft vinyl Disney character figurines because the arms or legs can detach, posing a choking hazard to children. About 16,140 units were sold nationwide through retailers including BuyBuy Baby and Amazon from May through December 2022.

    Product
    My First Mickey Mouse, Minnie Mouse, Buzz Lightyear, and Stitch Figurines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23123·2023-02-16

    Children's Nightgowns Recalled for Flammability Standard Violation

    Betsy & Lace children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 90,550 units sold online from March 2018 through September 2022.

    Product
    Children's nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0345-2023·2023-02-15

    Skinny Dipped Dark Chocolate Cashews Recalled for Undeclared Peanut

    Skinny Dipped is recalling Dark Chocolate Salted Caramel Cashews (3.5 oz pouches) due to undeclared peanut. Peanut is present in the product but not listed on the label, posing risk to consumers with peanut allergies.

    Product
    Skinny Dipped Dark Chocolate Salted Caramel Cashews, 3.5 oz, packaged in flexible plastic pouches inside cardboard cases. Ingredients: Cashews, Dark Chocolate (Unsweetened Chocolate Processed with Alkali, Cane Sugar, Cocoa Butter, Milk Fat, Sunflower Lecithin, Vanilla), White…
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-1101-2023·2023-02-15

    RipCord Syndesmosis Button suture may break during orthopedic surgery

    The RipCord Syndesmosis Button's pull suture can break when excessive tension is applied during orthopedic surgery. TriMed Inc. is recalling 76 units due to this structural failure risk.

    Product
    RipCord Syndesmosis Button, REF: STA001K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1078-2023·2023-02-15

    Medline Sterile Surgical Trays Recalled for Potential Blade Puncture of Packaging

    Medline Industries is recalling sterile procedural trays because blades in the kits may puncture the outer packaging, potentially compromising sterility.

    Product
    Sterile Procedural Trays, labeled as the following: a. ST. ANNE'S MAJOR BASIN SET UP b. SINGLE BASIN SET c. DOUBLE BASIN SET d. LAPAROTOMY BASIN e. ORTHOPEDIC CUSTOM BASIN SET f. OISC BASIN TRAY g. BASIN PACK h. BASIN SET i. SURGI START PACK j. PK, GEN-SET UP…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1097-2023·2023-02-15

    Sterile arthroscopy trays recalled for potential blade puncture risk

    Medline Industries recalls multiple sterile arthroscopy surgical trays because blades in the kits may puncture the outer foil packaging, potentially compromising sterility. Affected products were distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. KNEE ARTHROSCOPY CDS-LF b. ARTHROSCOPY CDS c. ARTHROSCOPY LV - EDOC PACK-LF d. ARTHROSCOPY PACK-LF e. ARTHROSCOPY PACK f. ARTHRO PACK-LF g. ARTHROSCOPY PACK-LF h. ARTHROSCOPY PACK-LF i. ARTHROSCOPY KNEE TRAY-LF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1091-2023·2023-02-15

    Sterile Surgical Trays Recalled for Potential Sterile Packaging Puncture

    Medline Industries recalls sterile surgical procedural trays because blades within the kits could puncture the sterile outer packaging, potentially compromising sterility during surgical use.

    Product
    Sterile Procedural Trays, labeled as the following: a. GYN-URO LAPSCP CDS-LF b. ROBOTIC CDS c. GYN LAPAROSCOPY CDS-LF d. GYN LAPAROSCOPY e. GYN LAPAROSCOPY CDS f. UNIVERSAL ROBOTIC ORLANDO g. GYN ROBOTIC CDS h. GYN LAPAROSCOPY CDS-1 i. CUH GYN LAPAROSCOPY CDS j.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1079-2023·2023-02-15

    Sterile Procedural Trays Recalled for Potential Blade Puncture of Packaging

    Medline Industries is recalling multiple sterile procedural trays because blades within the kits can potentially puncture the outer foil packaging, compromising sterility. The recall affects approximately 215,456 units distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. BASIN SET-UP PACK b. LAP CHOLE CDS c. MAJOR CDS d. UROLOGY MINOR CDS e. UROLOGY MAJOR CDS f. SINGLE BASIC CDS g. ORGAN RECOVERY CDS h. GENERAL ABD CDS i. BURN CDS j. MINOR k. MAJOR VASCULAR l. BASIC CORE CDS m. ROBOTIC…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1074-2023·2023-02-15

    Sterile Procedural Trays Recalled Due to Blade Packaging Puncture Hazard

    Medline Industries is recalling multiple sterile procedural trays because blades within the kits can puncture the outer foil packaging. The products were distributed worldwide.

    Product
    Sterile Procedural Trays, labeled as the following: a. LAPAROTOMY CDS-LF b. LAPAROSCOPY CDS-LF c. BASIC LAPAROSCOPY CDS d. LAPAROSCOPY CDS-LF e. GENERAL LAPAROSCOPY PROCEDURE f. LAP CHOLE CDS g. COLO-RECTAL CDS-LF h. MAJOR PROCEDURE-LF i. HYPOSPADIUS CDS j. LAPAROSCOPY-GENERAL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1071-2023·2023-02-15

    Medline Sterile Procedural Trays Recalled Due to Blade Puncture Risk

    Medline Industries is recalling sterile procedural trays (Rhinoplasty Pack, OSC Otology Pack-LF, and Rhyzotomy) distributed worldwide because sterile blades within the kits may puncture the outer foil layer of sterile packaging, potentially compromising sterility.

    Product
    Sterile Procedural Trays, labeled as the following: a. RHINOPLASTY PACK b. OSC OTOLOGY PACK-LF c. RHYZOTOMY
    Category
    Medical Device
    Distribution
    Distributed nationwide