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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Minimum severity

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

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34551–34575 of 40325

  • ModerateFDA (Devices)·Z-0100-2015·2014-10-29

    Gyrus Medical Recalls Sterile Surgical Forceps and Scissors Due to Seal Defects

    Gyrus Medical is recalling specific sterile surgical forceps and scissors because a packaging anomaly may compromise the sterile barrier.

    Product
    GYRUS ACMI, REF 3345 -Everest BiCOAG MOLly Forceps 5mm/45cm REF 3345PK - PKS MOLly Forceps 5mm/45cm REF 3640 -Everest BiCOAG Macro Jaw Forceps 5mm/45cm REF 3640PK- PKS Macro Jaw Forceps 5mm/45cm REF 3844- Everest BiCOAG LP Scissors 5mm/45cm REF 910010PK- PKS MOLly Forceps…
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-0122-2015·2014-10-29

    Siemens IMMULITE 1000 Cortisol Assay Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling specific lots of IMMULITE 1000 Cortisol Assay reagents due to confirmed positive bias on controls.

    Product
    IMMULITE /IMMULITE 1000 Systems COR Cortisol, REF/Catalog Number LKC01, SMN 10381388, IVD. For in vitro diagnostic use with the IMMULITE 1000 Systems Analyzers for the quantitative measurement measurement of cortisol (hydrocortisone, Compound F) in serum, as an aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0101-2015·2014-10-29

    Estill Medical Recalls Ultra Battery 1 for Insufficient Charging Capacity

    Estill Medical Technologies is recalling 6,886 Ultra Battery 1 units because they may not reach full charge capacity within the standard 60-minute charging period.

    Product
    Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeable power source for the Thermal Angel Blood and IV Fluid Infusion Warmer. The TA-UB1 battery was designed to provide sufficient power for the Thermal Angel to warm and deliver one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0046-2015·2014-10-22

    Kendall Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs

    FDA recalls 133,930 pairs of Kendall defibrillation electrodes because they are not compatible with specific Philips AED models.

    Product
    Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0043-2015·2014-10-22

    Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs

    FDA recalls 317,550 pairs of defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.

    Product
    Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation Electrodes, Radiotransparent Part Number: 22660R
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0081-2015·2014-10-22

    Siemens Clinitek Status+ Power Supply Adapters Recalled for Electric Shock Risk

    Siemens Healthcare Diagnostics is recalling approximately 4,200 external power supply adapters for the Clinitek Status+ urine analyzer due to damage that can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status+ The Clinitek Status systems is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0044-2015·2014-10-22

    Coviden Defibrillation Electrodes Recalled for Incompatibility with Philips AEDs

    Coviden LLC is recalling 9,850 pairs of Medi-Trace Cadence defibrillation electrodes because they are not compatible with Philips FR3 or FRx AEDs.

    Product
    Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes, Pre-connected Part Number: 22660PC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0048-2015·2014-10-22

    Philips HEARTSTART Electrode Pads Recalled for Incompatibility with AEDs

    Covidien is recalling Philips HEARTSTART Multifunction Electrode Pads because they are not compatible with Philips FR3 or FRx AEDs.

    Product
    Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0074-2015·2014-10-22

    Intuitive Surgical Recalls EndoWrist Stapler 45 Instruments

    Intuitive Surgical is recalling 1,034 EndoWrist Stapler 45 instruments because they may not be removable from tissue.

    Product
    EndoWrist Stapler 45 instrument for the da Vinci Si System Model Number: IS3000 Product Usage: For use with da Vinci Si System. The Intuitive Surgical Endoscopic Instrument Control System is intended to assist in the accurate control of Intuitive Surgical Endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2015·2014-10-22

    Siemens Clinitek Status Power Supply Adaptors Recalled for Electric Shock Risk

    Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer because they are damaged and can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status Power Supply Adaptor - Spare Part The Clinitek Status system is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0068-2015·2014-10-22

    Merge Healthcare Recalls eFilm Workstation Software Due to Image Selection Error

    Merge Healthcare is recalling eFilm Workstation versions 4.0 and 4.0.1 because a software defect may cause users to select the wrong patient study when using the thumbnail panel.

    Product
    eFilm Workstation 4.0 and 4.0.1. eFilm Workstation is one of the components of a PACS (Picture Archiving and Communications System). Product Usage: eFilm Workstation is a software application that is used for viewing medical images. eFilm Workstation receives digital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0075-2015·2014-10-22

    Biomet Recalls Discovery Elbow Humeral Trial Due to Incorrect Etching

    Biomet is recalling six Discovery Elbow Humeral Trials that were incorrectly manufactured as left-sided but etched as right-sided.

    Product
    Discovery Elbow Humeral Trial Product Usage: Biomet manufactures a variety of elbow joint replacement prostheses intended for primary and revision joint arthoplasty for use in cemented applications. Elbow joint replacement components include humeral and ulnar components…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0069-2015·2014-10-22

    Invivo Recalls Philips Expression MR200 MRI Patient Monitoring Systems

    Invivo Corporation is recalling 24 Philips Expression MR200 MRI Patient Monitoring Systems because they may fail to produce Non-Invasive Blood Pressure (NIBP) measurements.

    Product
    Philips Expression MR200 MRI Patient Monitoring System
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0082-2015·2014-10-22

    Siemens Clinitek Status Power Supply Adaptors Recalled for Shock Risk

    Siemens Healthcare Diagnostics is recalling external power supply adaptors for the Clinitek Status urine analyzer due to damage that can cause electric shock.

    Product
    External power supply adaptors that accompany Clinitek Status Connect System The Clinitek Status system is a urine analyzer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0066-2015·2014-10-22

    Arrow Select Kits Recalled Due to Potential Sterility Compromise

    Arrow International is recalling Select Kits and Maximal Barrier Precautions Kits containing BD Posiflush syringes because open seals may compromise sterility.

    Product
    Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) with BD Medical Posiflush 10mL Saline Flush Syringe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0079-2015·2014-10-22

    ArjoHuntleigh Recalls Spreader Bars for Ceiling Lifts Due to Hook Flexibility

    Arjo, Inc. is recalling 363 spreader bars for the Maxi Sky 2 Ceiling Lift because the hooks are too flexible to securely hold sling loops.

    Product
    Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Model 700-19425. Intended to be used for general transfers in hospitals.
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-0067-2015·2014-10-22

    Primus Medical Recalls AC Powered Adjustable Bed Frames

    Primus Medical LLC is recalling 1,726 AC powered adjustable bed frames used in nursing facilities because the head deck actuator bracket may separate from the frame.

    Product
    AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0070-2015·2014-10-22

    KCI Recalls V.A.C. GranuFoam Silver Dressing Due to Expiry Date Error

    KCI USA, Inc. is recalling V.A.C. GranuFoam Silver Dressing because some sterile pouches display an incorrect expiry date.

    Product
    V.A.C. GranuFoam Silver Large Dressing is barrier to bacterial penetration and may help reduce infection. Featuring SensaT.R.A.C. Technology REF M8275099/10 STERILE Single Use only Latex Free Rx Only.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0063-2015·2014-10-22

    Intuitive Surgical Recalls EndoWrist One Vessel Sealer for Labeling and Software Issues

    Intuitive Surgical is voluntarily correcting labeling and software for the EndoWrist One Vessel Sealer used with the da Vinci Si Surgical System.

    Product
    EndoWrist One Vessel Sealer used in conjunction with the da Vinci Si Surgical System IS3000. The Endo Wrist One Vessel Sealer is a bipolar electrosurgical instrument for use with the da Vinci Si Surgical System and the ERBE VIO 300 D electrosurgical generator. It is intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0073-2015·2014-10-22

    Ameditech Recalls ArcPoint Labs 10 Panel Dip Screen Due to Labeling Error

    Ameditech is recalling 320 kits of the ArcPoint Labs 10 Panel Dip Screen (OXY) because the positive interpretation illustration on the cap labels and package insert was incorrect.

    Product
    ArcPoint Labs 10 Panel Dip Screen (OXY), Part No. APD-10MO. The ArcPoint Labs Dip Drug Screen Dip Card is a one-step immunoassay for the qualitative detection of multiple drugs and drug metabolites in human urine.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0064-2015·2014-10-22

    Roche Omni Micro-electrode Recall for Inconsistent Reference Values

    Roche Diagnostics is recalling Omni Micro-electrodes for the cobas b221 analyzer because default reference values are inconsistent with other instruments and instructions.

    Product
    Omni Micro-electrode/reference electrode for cobas b221 analyzer. The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit, glucose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0071-2015·2014-10-22

    Ameditech Recalls ArcPoint Labs 5 Panel Dip Drug Screen Due to Labeling Error

    Ameditech is recalling 400 kits of the ArcPoint Labs 5 Panel Dip Drug Screen because the positive interpretation illustration on the labels and package insert was incorrect.

    Product
    ArcPoint Labs 5 Panel Dip Drug Screen, Part No. APD-5M. The ArcPoint Labs Dip Drug Screen Dip Card is a one-step immunoassay for the qualitative detection of multiple drugs and drug metabolites in human urine.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0078-2015·2014-10-22

    Ortho VITROS 5600 Integrated System Recalled for Calibration Anomaly

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems due to a software anomaly that may cause unexpected assay calibration when using specific calibrator kits.

    Product
    VITROS 5600 Integrated System, System Product Code 6802413. For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS Chemistry Products MicroTip Reagents…
    Category
    Medical Device
    Distribution
    Distributed nationwide