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.

Filters

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

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

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

Clear filters

22751–22775 of 40339

  • SevereFDA (Devices)·Z-2892-2018·2018-08-29

    Philips SureSigns VSV Monitors Recalled for Battery Overheating and Ignition Risk

    Philips is recalling SureSigns VSV monitors because lithium-ion batteries may overheat or ignite if not replaced on schedule, posing fire and injury risks.

    Product
    Philips SureSigns VSV (Vital Signs Viewer), 863067 Indicated for central monitoring of multiple adult, pediatric and neonatal patients, and where the clinician decides to monitor cardiac arrhythmia of adult, pediatric and neonatal patients to gain information for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2837-2018·2018-08-29

    Siemens 3D TOP Ceiling Stand Recalled for Potential Rope Failure

    Siemens Medical Solutions is recalling 699 3D TOP Ceiling Stands because a load-bearing rope could break, causing the arm to drop and potentially seriously injure patients or users.

    Product
    3D TOP Ceiling Stand, model no. 3070039 3074486 3070013 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the detector and is moveable on a ceiling rail system in three axis. The tube and / or detector can be rotated above a horizontal and a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2817-2018·2018-08-29

    bioMerieux VITEK 2 Gram Positive Test Kits Recalled for MRSA Detection Issues

    bioMerieux is recalling VITEK 2 Gram Positive Test Kits because customer reports indicated an increased rate of non-detected MRSA.

    Product
    bioMerieux VITEK 2 Gram Positive Cefoxitin Screen, VITEK 2 Gram Positive AST for Oxacillin, VITEK SYSTEMS General Susceptibility Card Cefotoxin and AST for Oxacillin bioMerieux VITEK 2 AST-P631 bioMerieux VITEK 2 AST-GP67 Test Kit bioMerieux VITEK 2 AST-GP71 Test Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2896-2018·2018-08-29

    Philips SureSigns VS2 Monitor Recall for Battery Overheating and Ignition Risk

    Philips is recalling SureSigns VS2 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing fire and injury risks.

    Product
    Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2 vital signs monitor is for use by healthcare professionals whenever there is a need for monitoring the physiological parameter of patients. Standard and optional parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2894-2018·2018-08-29

    Philips SureSigns VS4 Vital Signs Monitor Recalled for Battery Fire Risk

    Philips is recalling SureSigns VS4 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing injury and property damage risks.

    Product
    Philips SureSigns VS4 Vital Signs Monitor, 863283 863286 The SureSigns VS4 vital signs monitor is for use by healthcare professionals whenever there is a need for monitoring the physiological parameters of patients. The SureSigns VS4 monitor is for monitoring, recording…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2893-2018·2018-08-29

    Philips SureSigns VS3 Vital Signs Monitor Recall for Battery Fire Risk

    Philips is recalling SureSigns VS3 monitors because lithium-ion batteries may overheat or ignite if not replaced on time, posing fire and injury risks.

    Product
    Philips SureSigns VS3 Vital Signs Monitor, 863069 863070 863071 863072 863073 863074 The SureSigns VS3 monitor is for monitoring, recording and alarming of multiple physiological parameters of adults, pediatrics, and neonates in healthcare environments. Additionally, the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2838-2018·2018-08-29

    Siemens 3D V Ceiling Stand Recalled for Potential Rope Failure

    Siemens is recalling 3D V ceiling stands because the primary load-bearing rope could break, causing the arm to drop and potentially seriously injuring patients or users.

    Product
    3D V, model. no. 7042042 7042059 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the detector and is moveable on a ceiling rail system in three axis. The tube and / or detector can be rotated above a horizontal and a vertical axle. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2753-2018·2018-08-29

    Handicare P600 Series Patient Lift Recalled for Strap Wear and Breakage

    Handicare USA Inc. is recalling four P600 Series patient lifts due to premature strap wear and breakage at maximum weight conditions.

    Product
    Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2860-2018·2018-08-29

    Philips DigitalDiagnost Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost Rel.4 Upgrades because a defective hook may allow the footplate to fall or swing, potentially injuring patients or operators.

    Product
    DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2844-2018·2018-08-29

    Philips DigitalDiagnost Release 3 Footplate Hook Recall

    Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost Release 3 (Stitching Patient Support) 712025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2741-2018·2018-08-29

    Compass Health Brands Recalls CPAP Mask Cushions Due to Design Incompatibility

    Compass Health Brands is recalling CPAP mask cushions because a design change makes them incompatible with previous elbow parts, potentially causing unacceptable CO2 porting.

    Product
    CPAP Mask Cushion, Model Nos. PB781S, PB781M, PB781L, 781S, 781M and 781L Product Usage: A CPAP mask is attached to an end user s face and a CPAP machine, to treat end users with sleep apnea. The replacement cushion is a non-durable component that requires replacement every…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2842-2018·2018-08-29

    Philips DigitalDiagnost 4 Flex Footplate Recall Due to Injury Risk

    Philips is recalling two DigitalDiagnost 4 Flex units because a defective hook allows the footplate to fall, posing an injury risk to patients or operators.

    Product
    DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2861-2018·2018-08-29

    Philips DigitalDiagnost Release 3 Footplate Hook Recall for Injury Risk

    Philips is recalling DigitalDiagnost Release 3 units because a defective hook may allow the footplate to fall or swing, posing an injury risk to patients or operators.

    Product
    DigitalDiagnost Release 3 (Stitching Patient Support) 712025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2850-2018·2018-08-29

    Philips DigitalDiagnost 4 Flex Footplate Recall for Injury Risk

    Philips is recalling DigitalDiagnost 4 Flex and Value units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.

    Product
    DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2897-2018·2018-08-29

    Richard Wolf Artholine Punch B 4, 6MM H 1, 6MM Recalled for Potential Injury Risk

    Richard Wolf GmbH is recalling 12 units of Artholine Punch B 4, 6MM H 1, 6MM because a potential burr in the joint may increase the risk of injury when the device is opened.

    Product
    Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically created passages. Product Usage: Device is a standard punch; standard punches are used for the removal of soft tissue, cartilage…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2847-2018·2018-08-29

    Philips CombiDiagnost R90 Footplate Hook Recall for Injury Risk

    Philips is recalling CombiDiagnost R90 units because a defective hook may allow the footplate to fall, posing an injury risk to patients or operators.

    Product
    CombiDiagnost R90 (Stitching Patient Support) 709030
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2849-2018·2018-08-29

    Philips DigitalDiagnost 4 Chest Footplate Recall Due to Injury Risk

    Philips is recalling DigitalDiagnost 4 Chest units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2869-2018·2018-08-29

    BD BBL GC-Lect Agar Recalled Due to Incorrect Antibiotic Ingredient

    Becton Dickinson is recalling BD BBL GC-Lect Agar plates because some were made with Gentamicin instead of Vancomycin, which may cause false negative gonorrhea test results.

    Product
    BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better inhibition of contamination bacteria and fungi.
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-2873-2018·2018-08-29

    GE Healthcare Optima CT660 Systems Recalled for Damaged Cable Hazard

    GE Healthcare is recalling Optima CT660 systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.

    Product
    GE Healthcare Optima CT660. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold only outside the U.S. under the following product names: CT OPTIMA 660, CT OPTIMA 660 LONG BJG SKD RUS, CT OPTIMA 660 LONG BJG SKD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2840-2018·2018-08-29

    Elekta Digital Accelerator Recall for Potential Uncontrolled Detector Arm Extension

    Elekta is recalling 2,998 Digital Accelerators worldwide due to a potential for uncontrolled extension of iViewGT or XVI detector arms.

    Product
    ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise Digital Accelerator, Infinity, Axesse, and Versa HD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2858-2018·2018-08-29

    Philips DigitalDiagnost Dual Detector Footplate Recall for Injury Risk

    Philips is recalling DigitalDiagnost Dual Detector units because the footplate hook may fail, causing the plate to fall and injure patients or operators.

    Product
    DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2854-2018·2018-08-29

    Philips DigitalDiagnost 4.1 Flex Footplate Recall for Injury Risk

    Philips is recalling DigitalDiagnost 4.1 Flex and Value units because the footplate hook may fail, causing the footplate to fall and injure patients or operators.

    Product
    DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2870-2018·2018-08-29

    GE Healthcare Recalls CT Systems Due to Damaged Cable Electrical Hazard

    GE Healthcare is recalling specific CT systems because a damaged cable may expose 120VAC to service engineers working inside the gantry.

    Product
    GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. Sold under the following product names: CT GOLDSEAL LIGHTSPEED ULTRA, CT OPTIMA 660, CT OPTIMA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2839-2018·2018-08-29

    Hitachi Scenaria CT System Recalled for Table Motion Hazard

    Hitachi is recalling one Scenaria CT system in Texas because the patient table failed to stop and contacted the gantry, posing a risk of injury.

    Product
    Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomography applications in patients of all ages. The images can be acquired in either axial, helical, gated or dynamic modes. The volume…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2864-2018·2018-08-29

    Philips DigitalDiagnost Upgrades Recalled Due to Footplate Safety Hazard

    Philips is recalling DigitalDiagnost Upgrades because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.

    Product
    DigitalDiagnost Upgrades (Stitching Patient Support) 712083
    Category
    Medical Device
    Distribution
    Distributed nationwide