The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

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All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

19951–19975 of 90011

  • HighFDA (Devices)·Z-1397-2023·2023-04-26

    Habib EndoHPB Bipolar RF Catheter Recalled Due to Thermal Injury Risk

    Boston Scientific recalls the Habib EndoHPB Bipolar RF Catheter used in pancreatic and biliary procedures due to inaccurate instructions that could result in excessive energy delivery and thermal injury.

    Product
    Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A radiofrequency (RF) catheter which provides bipolar energy to perform partial or complete ablation of tissue in the pancreatic and biliary tracts. UPN: M00500070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1417-2023·2023-04-26

    Philips 2D Perfusion Medical Imaging Software Recalled for Signal Processing Errors

    Philips is recalling 2D Perfusion diagnostic imaging software due to signal processing errors that can produce inaccurate presentations, potentially affecting clinical decisions.

    Product
    2D Perfusion, release R1.0.x, R1.1.x, R1.2, and R1.2.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1399-2023·2023-04-26

    Tobii Dynavox TD I-110 Speech Device Recalled Over Loose Battery Risk

    The FDA is recalling the Tobii Dynavox TD I-110, a speech-generating device, because the battery may become loose from its housing and potentially be damaged. This affects users worldwide who depend on this device for communication.

    Product
    Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device used for ambulatory people with disabilities. Catalog #: 750567
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V294000·2023-04-26

    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 — BMW X7, XM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1394-2023·2023-04-26

    Radiometer AQURE Software Recall Due to Patient Mix-up Risk

    Radiometer is recalling AQURE laboratory software versions 2.5.2 through 2.6.1 due to a potential issue that could cause patient data mix-ups.

    Product
    AQURE REF 933-599 Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 The AQURE system is intended to let you manage analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0746-2023·2023-04-26

    Natural Pak Bacon Glaze Mislabeled; Contains Undeclared Coffee Chili Rub

    Victoria Gourmet's Natural Pak Bacon Glaze packages labeled and sold in Ohio actually contain Coffee Chili Rub with undeclared ingredients including mustard, an allergen.

    Product
    Natural Pak brand Bacon Glaze is packaged in 22.9oz (649g), white, cylindrical, plastic containers; Ingredients: Demerara sugar, honey granules, brown sugar, maple sugar, paprika, spices (black pepper, cinnamon, allspice, clove, natural flavors (maple, honey, cinnamon, clove)…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1420-2023·2023-04-26

    Baxter ExactaMed Oral Dispenser Recalled for Particulate Matter Contamination

    Baxter Healthcare Corporation is recalling the ExactaMed 20 mL Oral Dispenser (Lot B301S356P) because it may contain particulate matter. The recall affects approximately 91,100 units distributed in the US.

    Product
    ExactaMed Oral Dispenser - 20 mL Clear Pharmacy Pack, REF H9387120; Oral medication syringe
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1414-2023·2023-04-26

    Samsung GM85 Digital X-ray Imaging System Arm Latch Failure

    NeuroLogica Corporation recalls 935 Samsung GM85 digital X-ray systems due to a faulty arm latch in the column support that could allow the arm to fall, creating a risk of bodily injury.

    Product
    Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1407-2023·2023-04-26

    Surgical Centurion CirClamp Recalled for Incorrect Subassembly Size

    Medline Industries is recalling 162 units of Centurion CirClamp surgical devices due to incorrect subassembly size. The defect could affect proper device function during surgical use.

    Product
    Centurion CirClamp with 1.3cm Bell & Insert Reprocessed, Reorder #CR230K, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1402-2023·2023-04-26

    Medacta MectaLIF ANTERIOR spine implant recalled due to screw breakage risk

    Medacta USA is recalling MectaLIF ANTERIOR interbody fusion devices due to a potential for breakage of a small screw that secures the anti-backout plate. The defect affects 44 units distributed across five US states.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1418-2023·2023-04-26

    Olympus Single-Use Endoscopic Clip Fixing Device Recalled for Deployment Failure

    Olympus is recalling single-use rotatable clip fixing devices used in endoscopy procedures. The clips may fail to deploy from the tube sheath during use.

    Product
    Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model HX 201UR 135 - Rotatable, 230 cm long, 2.8 scope channel, standard clip Model HX 201UR 135L - Rotatable, 230 cm long, 2.8 mm scope channel, Long clip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1405-2023·2023-04-26

    Spinal fusion device antibackout screw may break, FDA recalls

    Medacta Usa Inc is recalling MectaLIF ANTERIOR antibackout lag covers due to potential breakage of the small screw that affixes the anti-backout plate. The defect affects spinal fusion procedures in select US states.

    Product
    MectaLIF ANTERIOR - Antibackout Lag Cover, REF 03.30.305, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·23V300000·2023-04-26

    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 — GENESIS GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1393-2023·2023-04-26

    Smith & Nephew Knee Implant Component Mispack: Wrong Size Distributed

    Smith & Nephew is recalling 12 JOURNEY II UNI Tibia Insert components due to a manufacturing mispack. Some boxes incorrectly contain a different size component.

    Product
    JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0538-2023·2023-04-26

    Compounded Semaglutide Injection Recalled Due to Sterility Assurance Failure

    Vital Care Compounder is recalling C-Semaglutide 5mg/mL injection in 0.5mL vials due to lack of assurance of sterility. The recall affects 45 vials distributed in Mississippi.

    Product
    C-Semaglutide 5mg/mL injection, 0.5mL vials, Rx only, Vital Care Compounder 115 South 40th Ave, Suite A Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1404-2023·2023-04-26

    Interbody Fusion Device Recalled for Potential Screw Breakage

    Medacta's MectaLIF ANTERIOR fusion device is being recalled due to potential breakage of a small screw used to affix the anti-backout plate. The recall affects 17 units distributed across the US.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H18, REF 03.30.304, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1411-2023·2023-04-26

    Spinal Implant Screws Recalled for Defective Titanium Material

    Medtronic is recalling INFINITY spinal implant screws manufactured with incorrect titanium material. The defect reduces the screw's gripping strength, risking implant performance in critical spinal fusion surgery.

    Product
    INFINITY Occipitocervical Upper Thoracic System, PARTIALLY THREADED MULTI AXIAL SCREW, Size: 4.0mm x 22mm, REF 360PT4022; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1415-2023·2023-04-26

    Laboratory diagnostic device software issue may delay clinical diagnosis

    BD Kiestra InoqulA+ (software versions 5.1/5.1.1) fails to display plate information after processing in clinical laboratories, risking diagnostic delays or specimen recollection.

    Product
    BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro diagnostic medical device intended to automate specimen processing according to user-defined procedures and protocols. Catalog (Ref) No.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1410-2023·2023-04-26

    Medtronic INFINITY Spinal Fusion Screws Recalled for Material Defect

    Medtronic is recalling 10 units of INFINITY Multi-Axial Screws distributed in the US and Canada because incorrect titanium material reduces gripping strength in affected lots.

    Product
    INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 32mm, REF 3604532; for immobilization and stabilization of spinal segment as an adjunct to fusion for the following acute and chronic instabilities of the craniocervical unction, the cervical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2023·2023-04-26

    FDA Recalls MectaLIF ANTERIOR Interbody Fusion Device Due to Screw Breakage Risk

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR interbody fusion device due to potential breakage of the small screw that affixes the anti-backout plate. The recall affects 34 units distributed in the United States.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1419-2023·2023-04-26

    Beckman Coulter Free T3 Reagent Test Kit Recalled for Falsely Elevated Results

    Beckman Coulter is recalling Access Free T3 reagent test kits (Catalog #A13422, Lot #233968) because approximately 15-20% of samples produce falsely elevated results that could lead to misdiagnosis and inappropriate thyroid treatment.

    Product
    Beckman Coulter Access Free T3, Triiodothyronine, Free, Catalog #A13422, each box contains 2 reagent packs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0733-2023·2023-04-26

    Dietary Supplement with Unapproved COVID-19 Treatment Claims Recalled

    Natural Solutions Foundation is recalling a colloidal silver dietary supplement labeled to treat COVID-19. The product violates FDA regulations prohibiting disease claims on dietary supplements.

    Product
    Dr. Rima Recommends The Silver Solution Immune System Support Dietary Supplement Nano Silver 10 ppm 16 fl. oz. (473 ml)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V292000·2023-04-25

    2023 Subaru Impreza Brake Light Switch and Transmission Interlock Defect

    Subaru is recalling certain 2023 Impreza vehicles due to a faulty brake light switch that may illuminate brake lights without pedal application and allow the transmission to shift out of PARK without pressing the brake pedal, creating rollaway and crash risk.

    Product
    SUBARU — SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-04252023-01·2023-04-25

    Ivars Ready-to-Eat Meat Soup Products Subject to Public Health Alert

    USDA FSIS issued a public health alert for Ivars meat soup products prepared under insanitary conditions. Consumers should not eat these items.

    Product
    Ivars Commissary — FSIS Issues Public Health Alert for Ready-to-Eat Meat Soup Products Due to Possible Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·23V293000·2023-04-25

    2022 Indian Chief Dark Horse motorcycles recalled for missing belt guard reflectors

    Indian Motorcycle Company is recalling certain 2022 Indian Chief motorcycles that lack belt guard reflectors, which reduces visibility and increases crash risk. All affected vehicles have been remedied.

    Product
    INDIAN — INDIAN CHIEF BOBBER, CHIEF BOBBER DARK HORSE, CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide