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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32276–32300 of 40325

  • SevereFDA (Devices)·Z-2264-2015·2015-08-12

    Medtronic Recalls EnVeo R Loading Systems Due to Particulate Presence

    Medtronic is recalling EnVeo R Loading Systems because of the presence of particulate. The recall affects 6,912 units worldwide, including 540 in the US.

    Product
    EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-C, LS-EnVeoR-2629-C. Cardiovascular valve delivery system for use with the Medtronic CoreValve Evolut R system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2331-2015·2015-08-12

    Siemens Biograph mCT S(40)-4R Recall for Missing Locking Ring

    Siemens is recalling one Biograph mCT S(40)-4R unit because it may be missing a locking ring on the optional ceiling mount.

    Product
    Biograph mCT S(40)-4R, Model Number 10248671
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2327-2015·2015-08-12

    Titan Spine Recalls Endoskeleton Locking Bone Screw Assemblies

    Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assemblies because the locking collars are not locking.

    Product
    Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; 5302-3516 / 03.5 x 16mm Locking Screws; 502-3518 / 03.5 x 18mm…
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2342-2015·2015-08-12

    Siemens Axiom Artis Angiography Systems Recalled for Liquid Seepage Risk

    Siemens Medical Solutions is recalling Axiom Artis angiography systems because liquid may seep through the top cover and penetrate internal components, potentially disabling table movements.

    Product
    Axiom Artis systems, dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2344-2015·2015-08-12

    Siemens ACUSON S Family Ultrasound Systems Recalled for Biopsy Guide Defect

    Siemens is recalling ACUSON S Family ultrasound systems because biopsy needles may move outside the on-screen guidelines when using specific attachments.

    Product
    ACUSON S Family ultrasound systems utilizing the 18L6 HD and/or 6C1 HD biopsy guidelines 6C1HD - model numbers: 10442008 6C1HD Needle Guide, S3000; 10440586 6C1 HD Biopsy Guide, S2000 18L6 - model numbers: 10442007 18L6 Biopsy Guide, S3000 10044200 S2000 Biopsy Starter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2340-2015·2015-08-12

    Siemens Artis zee Systems Recalled for Potential Liquid Seepage

    Siemens Medical Solutions is recalling Artis zee angiography systems because liquid may seep through the table cover, potentially preventing table movement.

    Product
    Siemens Artis zee systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2345-2015·2015-08-12

    Anspach Effort Recalls Synthes Oscillator Orthopedic Surgical Power Tools

    The Anspach Effort, Inc. is recalling Synthes Battery Power Line II Oscillator Model 530.710 units because the saw head may separate from the drive unit or come loose.

    Product
    Synthes Battery Power Line II Oscillator Model 530.710, orthopedic surgical power tool.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-2347-2015·2015-08-12

    Merge Hemo System Recalled for Freeze-Up During Cardiac Procedures

    Merge Healthcare is recalling 451 Merge Hemo systems used with Masimo PHASEIN modules due to system freeze-ups that required moving patients to other cath labs.

    Product
    Merge Hemo, 9.10, 9.20.0, 9.20.1,9.20.2, 9.30, 9.40.0, 9.40.1, 9.40.2 with Massimo PHASEIN End Tidal CO2 (EtCO2) module. Merge Hemo (formerly named HeartSuite Hemodynamics) monitors, measures, and records physiologic data from a human patient undergoing a cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2338-2015·2015-08-12

    Siemens Biograph 64-3R PET/CT Systems Recalled for Missing Locking Ring

    Siemens Medical Solutions is recalling Biograph 64-3R TruePoint systems because they may be missing a locking ring on optional ceiling mounts.

    Product
    Biograph 64-3R TruePoint w/ TrueV, Model Number 10097301
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2328-2015·2015-08-12

    Philips HeartStart XL+ Defibrillator Recalled for Software and Hardware Issues

    Philips is recalling 13,168 HeartStart XL+ defibrillators worldwide due to software and hardware issues that can affect device function.

    Product
    Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1991-2015·2015-08-12

    Olympus Analytical X-ray Systems Recalled for Higher Scatter Readings

    Olympus Scientific Solutions Americas is recalling 1,047 Analytical X-ray Systems because scatter readings around the probe head were higher than published specifications for certain samples.

    Product
    Olympus Scientific Solutions Americas Analytical X-ray System. Delta, Delta Element, Delta Plus, DPO-4000-XX-U-EN-EN-PM-SP12, DPO-6000-XX-U-EN-EN-AP-SP10. Mobile X-ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2337-2015·2015-08-12

    Siemens Biograph 64-4R CT Systems Recalled for Missing Locking Ring

    Siemens Medical Solutions USA Inc. is recalling two Biograph 64-4R CT systems because they may be missing a locking ring on optional ceiling mounts.

    Product
    Biograph 64-4R TruePoint w/ TrueV, Model Number 10097302
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2333-2015·2015-08-12

    Siemens Biograph mCT X-4R Systems Recalled for Missing Locking Ring

    Siemens Medical Solutions is recalling two Biograph mCT X-4R systems because they may be missing a locking ring on optional ceiling mounts.

    Product
    Biograph mCT X-4R, Model Number 10248670
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2349-2015·2015-08-12

    Zimmer Surgical Recalls Tourniquet Cuffs with Missing Instructions

    Zimmer Surgical Inc. is recalling 330 units of 30-inch tourniquet cuffs because the instructions for use were missing usage instructions and warnings.

    Product
    30inch Dual Port/Single Bladder Disposable Tourniquet Cuff with PLC, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder…
    Category
    Medical Device
    Distribution
    45 states
  • ModerateFDA (Devices)·Z-2341-2015·2015-08-12

    Siemens Artis Q Systems Recalled for Potential Liquid Ingress

    Siemens Medical Solutions is recalling Artis Q angiography systems because liquid may seep through the top cover, potentially disabling table movements. No injuries have been reported.

    Product
    Artis Q systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac angiography, neuro angiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2336-2015·2015-08-12

    Siemens Biograph 6-4R CT Systems Recalled for Missing Locking Ring

    Siemens Medical Solutions is recalling specific Biograph 6-4R CT systems because they may be missing a locking ring on optional ceiling mounts.

    Product
    Biograph 6-4R TruePoint w/ TrueV, Model Number 10097290
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2346-2015·2015-08-12

    Atrium 36Fr Right Angled Firm PVC Thoracic Catheter Recall

    Atrium Medical Corporation is recalling 620 units of 36Fr Right Angled Firm PVC Thoracic Catheters due to incorrect labeling on inner pouches.

    Product
    Atrium 36Fr Right Angled Firm PVC Thoracic Catheter, (Pkg of 10) Part Number: 15236
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-2330-2015·2015-08-12

    Roche Cobas b 221 S2 Fluid Pack Recall for Transponder Error

    Roche is recalling S2 Fluid Packs for the Cobas b 221 system because they may generate a transponder error, preventing the instrument from starting measurements.

    Product
    S2 Fluid Pack on the Cobas b 221 system- Catalog Number 03260925184 Blood Gas and Electrolytes 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…
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2339-2015·2015-08-12

    GE Healthcare Recalls MRI Scanners Due to Potential Image Orientation Errors

    GE Healthcare is recalling 82 MRI scanners because a missing spacer may cause images to be flipped left-right with incorrect orientation annotations.

    Product
    GE Healthcare, Signa Infinity MR System; Signa MR/i MR System; SmartSpeed; EchoSpeed Plus; HighSpeed Plus, Signa Infinity MR System with EXCITE Technology, Excite II, Signa 3T Infinity with Excite, Signa Excite 1.5T and Signa Excite 3T, Signa Excite HD, Signa HD 1.5T and Signa…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2348-2015·2015-08-12

    Zimmer Surgical Recalls Tourniquet Cuffs Due to Missing Instructions

    Zimmer Surgical Inc. is recalling 61 units of 18-inch disposable tourniquet cuffs because the folded instructions for use pamphlet was missing usage instructions and warnings.

    Product
    18inch Dual Port/Single Bladder Disposable Tourniquet Cuff, Zimmer Surgical, Inc. Tourniquets are intended to be used by qualified medical professionals to exert enough pressure on the arterial blood flow in a limb to produce a bloodless operating field. Single bladder…
    Category
    Medical Device
    Distribution
    45 states
  • SevereFDA (Devices)·Z-2209-2015·2015-08-05

    Skeletal Kinetics Recalls InjectionPlasty 1.0 Bone Void Filler Kits

    Skeletal Kinetics is recalling 67 kits of InjectionPlasty 1.0 Bone Void Filler due to reports of venous uptake, DVT, and pulmonary embolism in implanted patients.

    Product
    InjectionPlasty 1.0 Bone Void Filler; an injectable and biocompatible calcium phosphate bone void filler. Sterilized using irradiation. The single-use InjectionPlasty 1.0 Kit contains the necessary components for mixing and delivery of the bone void filler. The InjectionPlasty…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2271-2015·2015-08-05

    Draeger Fabius MRI Anesthesia Machine Recalled for Magnetic Field Attraction

    Draeger Medical is recalling 373 Fabius MRI anesthesia machines because their parts can be loosened by the magnetic field of MRI equipment.

    Product
    Fabius MRI Anesthesia Machine; Fabius MRI is an inhalation anesthesia machine for use in MRI environments in operating, induction and recovery rooms.
    Category
    Medical Device
    Distribution
    Distributed nationwide