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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17501–17525 of 27505

  • HighFDA (Devices)·Z-2517-2018·2018-08-01

    Implantcast Recalls Hip Implant Inserts Due to Retaining Ring Mounting Risk

    Implantcast GmbH is recalling specific 2M insert 15degree orthopedic hip implant components because the retaining ring may be incorrectly mounted.

    Product
    2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component. Size 38/39 mm REF number 02423839 Size 42/44 mm REF number 02424244 Size 44/48 mm REF number 02424448 Size 46/52 mm REF number 02424652
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2542-2018·2018-08-01

    Life Technologies Recalls Gibco CTS OpTmizer T Cell Expansion Medium

    Life Technologies is recalling Gibco CTS OpTmizer T Cell Expansion Serum Free Medium due to compromised fill port tube seals that may allow mold growth.

    Product
    Gibco CTS OpTmizer T Cell Expansion Serum Free Medium, bag format, Model Numbers A1048503 and A1022103. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2539-2018·2018-08-01

    Ad-Tech Drill Sleeve Guides Recalled Due to Raw Material Tolerance Defect

    Ad-Tech Medical Instrument Corporation is recalling 65 Drill Sleeve Guides because raw material diameter was under tolerance, which could cause drill bits to seize during surgery.

    Product
    AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the following lots from vendor 00-0001062., AD0021502, AD0021628. Product Usage: The drill sleeve guides are accessories to the Ad-Tech Cranial Drill Bits. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2532-2018·2018-08-01

    Ethicon Recalls PDS Plus Antibacterial Sutures Due to Tensile Strength Defect

    Ethicon, Inc. is recalling specific lots of PDS Plus Antibacterial Sutures because they do not meet tensile strength specifications.

    Product
    PDS Plus Antibacterial (Polydioxanone) Suture-PDS PLUS Undyed Suture 45cm (18") 4-0 Single Armed PS-4 Prime Needle Product Code: PDP507G (GTIN 10705031203983)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2535-2018·2018-08-01

    Elekta Recalls HexaPOD evo RT Couch Top for Positioning Errors

    Elekta, Inc. is recalling 725 HexaPOD evo RT Couch Top devices because they may tilt incorrectly after specific workflows, leading to improper patient positioning during radiation therapy.

    Product
    HexaPOD evo RT Couch Top (also known as HexaPOD evo Module), a component of the HexaPOD evo RT system. Product Usage: To support and aid in positioning a patient during radiation therapy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2544-2018·2018-08-01

    Life Technologies Recalls Gibco DMEM Tissue Culture Medium Due to Seal Defect

    Life Technologies is recalling Gibco DMEM tissue culture medium because compromised seal integrity may allow media to leak and grow mold.

    Product
    Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, pyruvate, Model Number 11995115. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2543-2018·2018-08-01

    Life Technologies Recalls GIBCO CTS AIM V Serum-Free Media Due to Seal Defect

    Life Technologies is recalling 141 units of GIBCO CTS AIM V Serum-Free Media because compromised seal integrity may allow media to leak and grow mold.

    Product
    GIBCO CTS AIM V Serum-Free Media (SFM), Model Number 0870112BK. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2549-2018·2018-08-01

    FDA Recalls Prevent G Safety Winged Blood Collection Sets Due to Leaks

    Guangzhou Improve Medical Instruments Co., Ltd. is recalling 200,000 Prevent G Safety Winged Blood Collection Sets in Kansas due to leak complaints.

    Product
    Prevent G Safety Winged Blood Collection Set Glide - Sterile/EO
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2537-2018·2018-08-01

    Forte Automation Patient Positioning System Recalled for Communication Failures

    Forte Automation Systems is recalling 13 patient positioning systems in California due to periodic communication failures with the accuracy filter that may not be indicated to the operator.

    Product
    Patient Positioning System with KRC2 controller using software versions 2.3.1 2.3.10 Product Usage: The patient positioning system is a SCARA designed robotic arm designed to position a patient for medical procedures prescribed by oncologists and others that require a high…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2546-2018·2018-08-01

    Life Technologies Recalls Gibco RPMI 1640 Medium Due to Seal Integrity Issues

    Life Technologies is recalling Lot 1930752 of Gibco RPMI 1640 Medium because compromised fill port tube seals may allow media to leak and mold to grow.

    Product
    Gibco RPMI 1640 Medium, Model Number 61870150. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2527-2018·2018-08-01

    GE MR Surgical Suite Option Recalled for Patient Transfer Mechanism Defect

    GE Medical Systems is recalling 54 MR Surgical Suite Option units because a defect in the table transfer release may cause an unexpected loss of function in the patient transfer mechanism.

    Product
    MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic resonance scanner (previously cleared K041476) can be used to produce head and whole body magnetic resonance images that are high resolution high signal-to-noise…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2557-2018·2018-08-01

    Roche Recalls cobas m 511 Hematology Analyzer for Discrepant Results

    Roche Diagnostics Hematology is recalling 17 cobas m 511 integrated hematology analyzers due to discrepant results in patients with severe microcytic anemia.

    Product
    cobas m 511 integrated hematology analyzer, Model Number 07261691190 Product Usage: The cobas m 511 integrated hematology analyzer is a quantitative, automated analyzer with cell locating capability. It is intended for in vitro diagnostic use by a skilled operator in the…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2545-2018·2018-08-01

    Life Technologies Recalls Gibco DMEM Tissue Culture Medium Due to Seal Defect

    Life Technologies is recalling 91 units of Gibco DMEM tissue culture medium because compromised fill port seals may allow media to leak and grow mold.

    Product
    Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, Model Number 11965175. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2526-2018·2018-08-01

    Siemens Artis zee Systems Recalled for Defective Cooling Unit Seals

    Siemens is recalling Artis zee angiography systems with specific Laird cooling units due to defective seals that may allow coolant to leak into electrical parts, potentially causing sudden system shutdowns.

    Product
    Artis zee systems with Laird Cooling Unit for SSFD: Material # 7555118. Artis is an angiography system developed for single and biplane diagnostic imaging and interventional procedures.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-2533-2018·2018-08-01

    Ethicon Recalls PDS Plus Antibacterial Sutures for Tensile Strength Defects

    Ethicon, Inc. is recalling 756 units of PDS Plus Antibacterial Sutures because they do not meet tensile strength specifications. The affected products were distributed in Japan.

    Product
    PDS Plus Antibacterial Suture-PDS PLUS Undyed Suture 45cm (18") 5-0 Single Armed P-3 Prime Needle Product Code: PDP493G (GTIN 10705031203945)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2547-2018·2018-08-01

    Life Technologies Recalls Gibco DMEM Cell Culture Medium Due to Seal Defect

    Life Technologies is recalling 70 units of Gibco DMEM cell culture medium because compromised fill port seals may allow media to leak and grow mold.

    Product
    Gibco Dulbecco's Modified Eagle Medium (DMEM), high glucose, pyruvate, Model Number 11995123. Tissue and cell culture medium.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2536-2018·2018-08-01

    Bard Medical Recalls Arctic Sun Temperature Management Systems Due to Wiring Defect

    Bard Medical Division is recalling 5,608 Arctic Sun 5000 Temperature Management Systems because an improper wiring connection may cause overheating and component failure.

    Product
    Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating system, indicated for monitoring and controlling patient temperature within a range of 32¿C to 38.5¿C (89.6¿F to 101.3¿F) in adult and pediatric patients of…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-2554-2018·2018-08-01

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation software due to erroneous beam profile parameters that may cause incorrect dose calculations in large or off-axis fields.

    Product
    RayStation Radiation Therapy Treatment Planning System, Model nos. 2.5, 3.5, 4.0, 4.3, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 7.0 Product Usage RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2528-2018·2018-08-01

    Medela Invia Motion Negative Pressure Wound Therapy System Recalled for Battery Error

    Medela Inc is recalling 778 units of the Invia Motion Negative Pressure Wound Therapy System because the device may display a battery missing error.

    Product
    Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model 087.4010); b. 15 Days Negative Pressure Wound Therapy (Model 087.4012); c. 60 Days Negative Pressure Wound Therapy (Model 087.4014); d. Endure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2555-2018·2018-08-01

    Leica M320 Microscope Systems Recalled for Gas Spring Bracket Failure

    Leica Microsystems is recalling 8,564 M320 Microscope Systems because screws holding the gas spring bracket may fail, causing the optics carrier to drop.

    Product
    Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419, 10448420, 10448485, 10448486 Product Usage: Intended use of this device is an optical instrument for magnifying and illuminating specimens. It can be applied…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2508-2018·2018-07-25

    Medtronic Tri-Staple 2.0 Intelligent Reloads Recalled for Missing Sled Component

    Medtronic is recalling Tri-Staple 2.0 Intelligent Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.

    Product
    Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 mm Vascular/Medium, Item Code SIG30AVM
    Category
    Medical Device
    Distribution
    Distributed nationwide