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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27601–27625 of 40233

  • ModerateFDA (Devices)·Z-1246-2017·2017-03-01

    Merge Eye Station Import Utility Recalled for Image Import Errors

    Merge Healthcare is recalling the Eye Station Import Utility because images were not importing properly and were imported under "unknown" due to a validation issue.

    Product
    Merge Eye Station Import Utility (ESIU) when used with Merge Eye Station and Merge Eye Care PACS. The firm name on the labeling is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1226-2017·2017-03-01

    BioMerieux ETEST XM256 Cefuroxime Recalled for Potential Performance Issues

    BioMerieux SA is recalling ETEST XM256 (Cefuroxime) antimicrobial susceptibility test strips due to potential performance issues that may result in false susceptibility or intermediate results.

    Product
    ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacterial such as Enterobacteriaceae, Pseudomonas, Staphylococcus and Enterococcus…
    Category
    Medical Device
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-1227-2017·2017-03-01

    Siemens N Latex HCY Reagent Recalled for Stability Issues

    Siemens Healthcare Diagnostics is recalling N Latex HCY Reagent kits due to reduced stability that may cause inaccurate homocysteine test results.

    Product
    N Latex HCY REAGENT, REF/Catalog OPAX03 /SMN 10445973 , IVD Product Usage: In-vitro diagnostic reagents for the quantitative determination of total homocysteine (HCY) in human serum, heparinized plasma and EDTA plasma by means of particle-enhanced immunonephelometry with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1248-2017·2017-03-01

    DeRoyal Heart Tracecart Recall Due to Sterile Component Packaging Issue

    DeRoyal is recalling Heart Tracecarts because they contain a sterile chest drainage product affected by a packaging configuration issue.

    Product
    SRHS DeRoyal Heart Tracecart REF 53-1913, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1231-2017·2017-03-01

    Quidel Recalls Influenza Transport Swab Packages Due to Incorrect Swabs

    Quidel Corporation is recalling Influenza Transport Swab Packages because they may contain incorrect sample swabs mixed with the proper ones.

    Product
    Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs in dry transport tubes are intended for use with influenza tests
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1243-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling 3,462 Dyonics Saw Blades, Narrow (Product Number 3705) because the single-use sterile devices lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1247-2017·2017-03-01

    DeRoyal Heart Tracecart Recall Due to Contained Chest Drainage Product Issue

    DeRoyal Industries is recalling Heart Tracecarts because they contain a Maquet Getinge chest drainage product affected by a separate packaging recall.

    Product
    DeRoyal Heart Tracecart REF 53-1769, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1241-2017·2017-03-01

    Smith & Nephew Recalls Dyonics Saw Blades Due to Missing Expiration Dates

    Smith & Nephew is recalling 4,500 Dyonics Saw Blades, Short (Product Number 3703) because the single-use sterile devices lack expiration dates on their labels.

    Product
    Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1223-2017·2017-03-01

    Applied Medical Technology Recalls Nasal Tube Retaining Systems Due to Expired Dates

    Applied Medical Technology is recalling 110 units of the AMT Bridle Nasal Tube Retaining System because expired expiration dates are listed on the pouches.

    Product
    AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Devices)·Z-1237-2017·2017-03-01

    Hidrex USA DVP1000 Recalled Due to Documentation Requirements

    Hidrex GmbH is recalling 180 units of the Hidrex USA DVP1000 device because it was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Hidrex USA DVP1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1224-2017·2017-03-01

    Applied Medical Technology Recalls Expired Feeding Sets

    Applied Medical Technology is recalling 110 units of AMT 12-inch Right Angle Feeding Sets with Y-Ports due to expired expiration dates listed on the pouches.

    Product
    AMT 12 inch Right Angle Feeding Set with Y-Port Used with Nasogastric/Nasointestinal (NG/NI) tubes.
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Devices)·Z-1236-2017·2017-03-01

    Hidrex USA DP450 Medical Device Recalled for Documentation Requirements

    Hidrex GmbH is recalling 64 units of the Hidrex USA DP450 device because it was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Hidrex USA DP450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1238-2017·2017-03-01

    Hidrex Recalls Daavlin Aquex Devices Due to Documentation Requirements

    Hidrex GmbH is recalling 250 Daavlin Aquex (DAAV1000) devices nationwide because the device was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Daavlin Aquex (DAAV1000)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1188-2017·2017-02-22

    GE Healthcare Recalls Discovery MR450 MRI Scanners Due to Burn Risk

    GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.

    Product
    Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1192-2017·2017-02-22

    Integra Cadence Total Ankle System Recalled Due to Tibial Fractures

    Integra LifeSciences Corp. is recalling 944 units of the Cadence Total Ankle System because posterior tibial fractures have been reported.

    Product
    Integra Cadence Total Ankle System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1123-2017·2017-02-22

    Physio-Control Recalls LIFEPAK 15 Defibrillators Due to Relay Failure

    Physio-Control is recalling 338 LIFEPAK 15 defibrillators because an internal relay may fail, preventing the device from delivering defibrillation energy.

    Product
    LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1215-2017·2017-02-22

    Siemens PRIMUS Radiation Therapy Systems Recalled for Collimator and Weld Defects

    Siemens is recalling 194 PRIMUS radiation therapy systems due to incorrect collimator position displays and improper weld seams at the overhead suspension.

    Product
    PRIMUS Medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1193-2017·2017-02-22

    Stryker Restoris RIO Reamer Handle Recalled for Engagement Failure

    Mako Surgical Corporation is recalling 595 Stryker Restoris RIO Reamer Handles because they may fail to engage mating components during surgery.

    Product
    Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components during acetabular reaming in MAKO Total Hip procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1103-2017·2017-02-22

    Zimmer Biomet Recalls Reverse Shoulder Humeral Trays Due to Fracture Risk

    Zimmer Biomet is recalling 4,388 Comprehensive Reverse Shoulder System Humeral Trays because they are fracturing at higher-than-anticipated rates, posing a risk of revision surgery.

    Product
    Comprehensive Reverse Shoulder System Humeral Tray Model 115340
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1194-2017·2017-02-22

    Argon Medical Devices Recalls Bone Marrow Aspiration Needles Due to Sterility Risk

    Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.

    Product
    BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone marrow specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2017·2017-02-22

    Terumo Recalls Hercules 360 Universal Stabilizing Arms Due to Pin Separation

    Terumo CVS is recalling Hercules 360 Universal Stabilizing Arms because pins may come loose and fall into the surgical site.

    Product
    Hercules 360 Universal Stabilizing Arm, top mount, 360-degree rotation, reusable stainless steel
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1218-2017·2017-02-22

    Aesculap GN200 Caiman HF Generators Recalled for Faulty Component

    Aesculap Implant Systems LLC is recalling 24 GN200 Caiman HF generators due to a faulty component that may impact proper device functioning.

    Product
    GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1219-2017·2017-02-22

    Zimmer Biomet Recalls Vanguard Total Knee Plates Due to Material Inclusions

    Zimmer Biomet is recalling Vanguard Total Knee punch-through trial plates due to potential alumina inclusions in the raw material that could cause the instruments to crack or separate.

    Product
    Vanguard Total Knee, PUNCH THRU TRL PLATES, 63 MM Item No: 32-487261, 67 MM Item No: 32-487262, 71 MM Item No: 32-487263, 75 MM Item No: 32-487264, and 79 MM Item No: 32-487265
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1206-2017·2017-02-22

    Atrium Medical Recalls Maquet Ocean Water Seal Chest Drains

    Atrium Medical Corporation is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after use.

    Product
    Maquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity or mediastinum. " To help re-establish lung expansion and restore breathing dynamics. " To facilitate postoperative collection and…
    Category
    Medical Device
    Distribution
    Distributed nationwide