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

Agency

Category

Minimum severity

Clear filters

37801–37825 of 40449

  • HighFDA (Devices)·Z-1956-2013·2013-08-21

    Medtronic Navigation Recalls Framelink Software Version 5.4 for Measurement Discrepancies

    Medtronic Navigation is correcting Framelink software version 5.4 due to potential discrepancies between exam images and displayed measurements during surgical planning.

    Product
    StealthStation S7 Framelink Software version 5.4. Aid for locating anatomical structures and planning surgical trajectories in open and percutaneous procedures.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1948-2013·2013-08-21

    Ortho-Clinical Diagnostics Recalls Worn CM/RT Incubator Wear Pads

    Ortho-Clinical Diagnostics is recalling Colorimetric (CM)/ Rate (RT) incubator wear pads because they may become worn before their scheduled replacement.

    Product
    Colorimetric (CM)/ Rate (RT) incubator wear pads. Product Codes: 1) 6801375, 2) 6801890, 3) 6802445, 4) 6802413 Product Usage: The CM/RT incubator processes Microslide reagents with the following VITROS systems: 1) VITROS 5,1 FS Chemistry System, 2) VITROS 5,1 FS Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1938-2013·2013-08-21

    Atrium Medical Recalls C-QUR V-Patch Mesh Due to Adhesion Issues

    Atrium Medical Corporation is recalling C-QUR V-Patch Mesh units because the coated mesh may adhere to the inner packaging liner when exposed to high humidity.

    Product
    C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2013·2013-08-21

    SpineFrontier Recalls Surgical Case Lids and Bases Due to Ink Delamination

    SpineFrontier, Inc. is recalling specific surgical case lids and bases because non-toxic inks used on the graphics are delaminating or running off after repeated washing and sterilization cycles.

    Product
    Case Lid and Base (Inspan, Invue, SLIFT) Caddy Lid (Inspan, Arena-C); Inspan Lid: 12-60039A, 11-60042B, 11-60043B, 11-60045B, 11-60046C, 11-60045A, 11-60046A, 11-60053A; Invue Lid: SI70095A; S-Lift Lid: SI50070A; S-Lift Base: SI50067A; Arena-C Lid: 11-72013D, 11-72014D…
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1975-2013·2013-08-21

    Siemens syngo.plaza Mammography Software Recall for Image Alignment Issues

    Siemens is recalling syngo.plaza software due to potential issues with mammography image laterality and alignment.

    Product
    Siemens syngo.plaza SW version VA20 with Mammography license. image processing, radiological system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1937-2013·2013-08-21

    Atrium Medical Recalls C-QUR Edge Mesh Due to Packaging Adhesion

    Atrium Medical is recalling C-QUR Edge Mesh products because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.

    Product
    C-QUR Edge Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1968-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recalled for Incomplete Operator Manual Instructions

    Terumo is recalling 1,657 Advanced Perfusion System 1 units because the operator manual does not fully describe pump behavior during specific alarm conditions.

    Product
    Terumo¿ Advanced Perfusion System 1: 100/120V AC, Advanced Perfusion System 1 The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1977-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recalled for False Pressure Alarm

    Terumo is recalling 1,657 Advanced Perfusion System 1 units because a false high-pressure alarm can stop the pump. The company is updating manuals and issuing labeling addenda.

    Product
    100/120V AC, Advanced Perfusion System 1 Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1934-2013·2013-08-21

    Medtronic Xomed Recalls ENT Surgical Instrument Trays for Labeling Defects

    Medtronic Xomed is recalling 3,562 ENT surgical instrument trays to replace them with units featuring improved 'PREVACUUM ONLY' labeling.

    Product
    Tray Surgical, ENT (various instrument trays) Used for stot age and transportation of reusable surgical instruments utilized in various ear, nose and throat (ENT) and head and neck surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1978-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recall for Pressure Alarm Issue

    Terumo is recalling 1,657 Advanced Perfusion System 1 units to update manuals and address a false high-pressure alarm that can stop the pump.

    Product
    220/240V AC, Advanced Perfusion System 1 Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1935-2013·2013-08-21

    Synthes Recalls 5.0mm Stainless Steel Spinal Rods Due to Process Error

    Synthes USA is recalling 492 units of 5.0mm stainless steel spinal rods because they were produced using a finishing process not identified in the manufacturing specification.

    Product
    5.0mm Unit Rod 270mm 5.0mm Unit Rod 290mm 5.0mm Unit Rod 310mm 5.0mm Unit Rod 330mm 5.0mm Unit Rod 350mm 5.0mm Unit Rod 370mm 5.0mm Unit Rod 390mm 5.0mm Unit Rod 410mm 5.0mm Unit Rod 430mm 5.0mm Unit Rod 450mm pedicle screw spinal system; Intended to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1973-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recalled for False Pump Service Error

    Terumo is recalling Advanced Perfusion System 1 units because user-induced movement may trigger a false 'Service Pump' error message, potentially causing unnecessary service delays.

    Product
    Terumo¿ Advanced Perfusion System 1 (APS1, System 1) 100/120V AC Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1945-2013·2013-08-21

    Siemens AXIOM Artis zeego x-ray system safety notice issued

    Siemens issued a customer safety notice regarding system information overlays after brake functional checks on the AXIOM Artis zeego x-ray system.

    Product
    Siemens AXIOM Artis zeego x-ray, angiographic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1965-2013·2013-08-21

    Arrow International Recalls Two-Lumen CVC Kits Due to Labeling Error

    Arrow International is recalling 156 Two-Lumen CVC Kits because a portion of the packaging incorrectly identifies the catheter as 3-Lumen.

    Product
    Arrow International, Inc. Two-Lumen CVC Kit with Blue Flex Tip Catheter. The multiple lumen catheter permits venous access to the central circulation of patients.
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1974-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recalled for False Service Pump Error Messages

    Terumo is recalling 1,657 Advanced Perfusion System 1 units because user-induced motor movement can trigger a false 'Service Pump' error message, potentially misleading operators.

    Product
    Terumo¿ Advanced Perfusion System 1 (APS1, System 1) Description: 220/240V AC Product Usage: The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1969-2013·2013-08-21

    Terumo Advanced Perfusion System 1 Recall for Incomplete Operator Manual

    Terumo is recalling 1,657 Advanced Perfusion System 1 units because the operator manual does not fully describe pump reactions during specific alarm conditions.

    Product
    Terumo¿ Advanced Perfusion System 1: 220/240V AC, Advanced Perfusion System 1 The Terumo¿ Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1936-2013·2013-08-21

    Atrium Medical Recalls C-QUR Mesh Due to Packaging Adhesion Issues

    Atrium Medical Corporation is recalling C-QUR Mesh products because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.

    Product
    C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1955-2013·2013-08-21

    Fisherbrand Sterile Swabs Recalled Due to Non-Pathogenic Organisms

    Fisher Scientific is recalling Fisherbrand Sterile Swabs after customer complaints reported non-pathogenic organisms in two lots.

    Product
    Fisherbrand Sterile Swab, Calcium Alginate Fiber Tipped, Wood Applicator Swab 100 pouches/boxes, 10 boxes/case. Used in applying medications to or take specimens from a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1941-2013·2013-08-21

    OrthoPediatrics Recalls 2.5mm Drill Bits Due to Packaging Labeling Error

    OrthoPediatrics is voluntarily recalling 68 packaged 2.5mm drill bits because the packaging incorrectly lists the size as 3.2mm.

    Product
    3.2mm Drill Bit. This is a component within the PediLoc Locking Plate System utilized to pre-drill a hole in bone prior to placement of a bone screw.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1960-2013·2013-08-21

    Biomet 3i Dental Implant Recall Due to Outer Box Mislabeling

    Biomet 3i is recalling 51 dental implants because outer boxes may be mislabeled. The implants themselves are correctly labeled, but the error could prevent proper placement.

    Product
    Biomet 3i Dental Implant, Parallel Walled 6mm (D) x 10mm (L)
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1961-2013·2013-08-21

    Biomet 3i Dental Implant Recall for Potential Outer Box Mislabeling

    Biomet 3i is recalling 33 dental implants because outer boxes may be mislabeled. The inner trays are correctly labeled, but the error could prevent proper implant placement.

    Product
    Biomet 3i Dental Implant, Non-Platform Switched Parallel Walled Implant 5mm (D) x 13mm (L)
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1946-2013·2013-08-21

    Stryker Recalls IsoGel AIR 84 Support Surfaces Due to Air Pump Alarm Issues

    Stryker is recalling 586 IsoGel AIR 84 support surfaces because connected air pumps may flash and alarm due to pressure blockages.

    Product
    IsoGel AIR 84, Support Surface. Intended to assist in improving human patient outcomes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1939-2013·2013-08-21

    Atrium Medical Recalls C-QUR TacShield Mesh Due to Packaging Adhesion

    Atrium Medical Corporation is recalling C-QUR TacShield Mesh units because the coated mesh can adhere to the inner packaging liner when exposed to high humidity.

    Product
    C-QUR TacShield Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1944-2013·2013-08-21

    GE Healthcare Recalls LOGIQ S8 Ultrasound Systems for Measurement Errors

    GE Healthcare is recalling 755 LOGIQ S8 Ultrasound Systems due to a software issue that may cause incorrect image measurements in Virtual Convex mode.

    Product
    GE Healthcare, LOGIQ S8 Ultrasound System The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1962-2013·2013-08-21

    Remel Flu A&B Control Swabs Recalled for Incorrect Quality Control Results

    Remel Inc is recalling Flu A&B Control Swabs because they may provide incorrect negative results for Flu A, potentially compromising quality control testing.

    Product
    Remel X/pect Flu A&B Control Swabs, For In Vitro Diagnostic Use, Ref R246003, each package contains 20 Flu A Control Swabs and 20 Flu B Control Swabs, each swab is individually packaged in a foil pouch. The firm name on the label is Remel Europe, Ltd., Dartford, Kent, United…
    Category
    Medical Device
    Distribution
    Distributed nationwide