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.

8451–8475 of 22105

  • HighFDA (Devices)·Z-1040-2025·2025-02-05

    Medline Procedure Kits Recalled for Surgical Mask Bioburden Testing Failure

    Medline has recalled 749 procedure kits containing surgical masks that failed to meet bioburden testing standards under EN 14683. The affected kits were distributed nationwide.

    Product
    Medline procedure kits labeled as: 1) Port Access Kit, Reorder number CVI5130; 2) VANTEX 7FR 3L 20CM CVC STOCK+ BUNDLE US. Reorder number STCVC01USGV; general surgical tray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0457-2025·2025-02-05

    Mustard Products Recalled Due to Salmonella in Seeds

    Keith Valley and Red Boy brand mustards distributed in the South and Southwest are being recalled because mustard seeds tested positive for Salmonella. Consumers should not consume affected products.

    Product
    Keith Valley mustard, net 1 gal, Distributed by: Ben E Keith Food Ft Worth, TX, UPC 046045062467; Red Boy brand mustard, Net 1 GAL., Distributed by Clements Food Company Oklahoma City, OK 73116, UPC 071735128154
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0440-2025·2025-02-05

    Cobb Salad Recalled Due to Potential Salmonella Contamination

    GBC Food Services is recalling Individual Cobb Salad products due to potential Salmonella contamination. The affected products were distributed in Colorado with purchase dates between November 22–29, 2024.

    Product
    Individual Cobb Salad 850054894632 11 oz (311g)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1036-2025·2025-02-05

    Medical stent delivery system outer sheath component detachment prevents proper expansion

    The HOT AXIOS Stent delivery system's outer sheath tip may detach during use, preventing proper stent expansion and requiring device exchange. Boston Scientific is recalling 1,102 units distributed nationwide.

    Product
    HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1025-2025·2025-02-05

    AXIOS Stent Delivery System: Detaching Outer Sheath May Prevent Stent Expansion

    Boston Scientific is recalling 1,144 AXIOS Stent Delivery System units because the outer sheath's distal black tip can detach. If this occurs, the tip may remain around the stent saddle and prevent proper stent expansion, requiring device exchange.

    Product
    AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx10mm UPN: M00553650
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1039-2025·2025-02-05

    Knee Implant Component Recalled for Incorrect Metal Post Assembly

    Zimmer, Inc. is recalling 155 units of NexGen LCCK Legacy knee implant components because the metal support post was assembled incorrectly in some units. The defective assembly could compromise implant function.

    Product
    NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E,F - Height 10 mm, Item Number 00-5994-032-10
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1067-2025·2025-02-05

    Implantable VNS Therapy Generators May Stop Delivering Treatment

    LivaNova is recalling approximately 8,223 SenTiva VNS Therapy generators due to a potential internal component failure that may cause the implanted device to stop delivering seizure therapy. Affected patients should contact their physician.

    Product
    Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA Product Description: The LivaNova VNS Therapy" System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy generator, lead, and exte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0456-2025·2025-02-05

    BakeMark USA Recalls Bavarian Creme Filling Due to Thermal Processing Deviation

    BakeMark USA recalls WESTCO 3065 Golden Bavarian Creme Filling due to a thermal processing deviation that may result in inadequate heat treatment. The product was distributed to 22 states.

    Product
    WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch, Contains 2% or Less of: Artificial Flavor, Salt, Color (Titanium Dioxide, Yellow 5, Yellow 6), Preservatives (Sodium Benzoate, Sorbic Acid, Potassium Sorbate, Phosphor
    Category
    Food
    Distribution
    22 states
  • HighNHTSA·24V338000·2025-02-05

    2024 Kia EV9 Front Passenger Seat Belt Retractor May Fail

    Kia is recalling certain 2024 EV9 vehicles because the front passenger seat belt retractor cover may not be properly secured, which can prevent the seat belt from locking correctly during a crash.

    Product
    KIA — 2024 KIA EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1037-2025·2025-02-05

    HOT AXIOS Stent System Recalled Due to Outer Sheath Detachment Risk

    Boston Scientific is recalling HOT AXIOS Stent systems due to potential outer sheath detachment that can prevent proper stent expansion. This defect may require device replacement during the procedure.

    Product
    HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 15mmx15mm UPN: M00553570
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0432-2025·2025-02-05

    Diced Bartlett Pears recalled for potential foreign object contamination

    Pacific Coast Producers is recalling diced Bartlett pears in syrup due to potential contamination with foreign objects. The affected product was distributed in Kentucky, Michigan, Ohio, and Pennsylvania.

    Product
    Diced Bartlett Pears In Extra Light Syrup, 105 OZ (6 LB 9 OZ), packed in a metal can, hermetically sealed
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1021-2025·2025-02-05

    Design Options Combined Spinal/Epidural Tray Recalled for Connector Defect

    B. Braun Medical is recalling 1,090 units of the Design Options Combined Spinal/Epidural Tray due to an incorrect catheter connector that cannot securely connect to the epidural catheter, preventing medication administration.

    Product
    Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal space and epidural space for pain control. Model/Catalog Number: 530159
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V294000·2025-02-04

    2023 BMW X7 and XM Recalled for Loose Exhaust-to-Catalytic Converter Fasteners

    BMW is recalling 2023 X7 and XM models due to improperly tightened fasteners connecting the exhaust system to the catalytic converter, which could increase fire risk. Dealers will replace the gasket and tighten fasteners at no charge.

    Product
    BMW — 2023 BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V298000·2025-02-04

    2023 Kia Sportage and Related Vehicles Instrument Cluster Display Failure

    The instrument cluster display in certain 2023 Kia vehicles may fail to show any information when started, preventing drivers from viewing critical safety data like tire pressure and warning lights. Kia will update the software for free.

    Product
    KIA — 2023 KIA SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V300000·2025-02-04

    2023 Genesis GV60 Rear Driveshaft Fracture Increases Crash Risk

    2023 Genesis GV60 vehicles with all-wheel drive may have rear driveshafts that fracture, resulting in loss of drive power and increased crash risk. Hyundai will replace the affected driveshafts at no cost to owners.

    Product
    GENESIS — 2023 GENESIS GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V201000·2025-02-03

    Jaguar E-Pace Brake Pad Warning Light May Not Activate

    Jaguar is recalling certain 2021-2024 E-Pace vehicles because the brake pad wear warning light may not appear when brake pads are worn. This could reduce braking ability and increase crash risk.

    Product
    JAGUAR — 2024 JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V197000·2025-02-03

    2022 RAM ProMaster Wiring Harness Causes Left Taillight and Turn Signal Failure

    Chrysler is recalling 2021-2022 RAM ProMaster vehicles due to wiring harness defects that can disable the left taillight and turn signal, increasing crash risk. Dealers will replace the harness free of charge.

    Product
    RAM — 2022 RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V200000·2025-02-03

    2022-2024 Kia EV6: Loss of Drive Power from Charging System Failure

    Kia is recalling 2022-2024 EV6 vehicles because the Integrated Charging Control Unit may fail, stopping the 12-volt battery from charging. This loss of drive power increases crash risk.

    Product
    KIA — 2022 KIA EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V001000·2025-02-01

    Aston Martin Vehicles Recalled: Infotainment Display Obstructs Rearview Camera

    Aston Martin is recalling certain 2024-2025 DB12, Vantage, and DBX707 vehicles. The infotainment home screen menu may obstruct the rearview camera when in reverse, reducing rear visibility and increasing the risk of a crash.

    Product
    ASTON MARTIN — 2024 ASTON MARTIN DB12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V030000·2025-02-01

    Jaguar I-PACE vehicles recalled for insufficient pedestrian warning sounds

    Jaguar is recalling 2021-2022 I-PACE vehicles because they fail to produce sufficient pedestrian warning sounds when stationary or in reverse, violating federal safety standards. Dealers will update the audio amplifier software at no charge.

    Product
    JAGUAR — 2022 JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V031000·2025-02-01

    Land Rover Range Rover Sport PHEV Pedestrian Warning Sound Defect

    Land Rover is recalling certain 2020-2022 Range Rover PHEV and Range Rover Sport PHEV vehicles because they fail to make sufficient warning sounds when stationary and in reverse, violating federal safety standards for hybrid and electric vehicles.

    Product
    LAND ROVER — 2021 LAND ROVER RANGE ROVER SPORT PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25111·2025-01-30

    Digital Kitchen Scales Recalled for Coin Battery Ingestion Risk

    Greater Goods digital kitchen scales with easily accessible lithium coin batteries violate federal safety regulations due to missing child-resistant packaging and warnings. Ingestion of coin batteries can cause serious injury or death; no incidents have been reported.

    Product
    Greater Goods Digital Kitchen Scales
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25113·2025-01-30

    Girls pajamas recalled due to flammability regulation violation, burn-injury risk

    Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.

    Product
    Cozchique, Tebbis and Beeziac Girls Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide