Medical devices, 2020
Shortlist up to four to read them side by side.
3,055 medical device recalls FDA’s Enforcement Report published in 2020, newest first; 40,450 in all since 2012.
FDA’s medical device recalls, as its Enforcement Report classifies them, from June 2012. Lists of FDA’s records can’t be saved for alerts: openFDA asks that its data not be used to alert the public (openFDA); FDA’s own emails do that. Copied Nov 6, 2026.
3,055of 3,055 medical device recallsshown with your filters
The list
- Medical device recall Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Hemashield Gold Knitted Microvel Double Velour Vascular Graft-Axillo-bifemoral Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Hemashield Gold Knitted Microvel Double Velour Vascular Graft Axillo-bifemoral Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-1 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft01 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-3 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft- 4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-4 Branch Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Probe, 9 FR AUTOLITH As part of an investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AUTOLITH URO-TCH 9FR PROBE 54CM Investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ACMI 9FR PROBE (E4-9F) Investigation into a biocompatibility test discrepancy where a lot failed biocompatibility testing. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. The filter installed onto the tube set may have the incorrect pore size. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and Alaska, California, Illinois, Kansas, Massachusetts, Missouri and South Dakota named
- Medical device recall Inpeco FlexLab Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware Versions:… The FlexLab Centrifuge Module loading algorithm may lead to unbalanced loads which could damage the centrifuge. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report27 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusOngoingWhereAlabama, California, Connecticut, Delaware, Florida, Iowa, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia and Washington
- Medical device recall Abbott Accelerator a3600 Centrifuge Module tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware… The FlexLab Centrifuge Module loading algorithm may lead to unbalanced loads which could damage the centrifuge. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report27 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusOngoingWhereAlabama, California, Connecticut, Delaware, Florida, Iowa, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia and Washington
- Medical device recall Siemens Aptio Automation Centrifuge Module, tube loading algorithm, Inpeco SA P/N: FLX-202, with Firmware… The FlexLab Centrifuge Module loading algorithm may lead to unbalanced loads which could damage the centrifuge. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report27 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusOngoingWhereAlabama, California, Connecticut, Delaware, Florida, Iowa, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Rhode Island, Tennessee, Texas, Virginia and Washington
- Medical device recall daVinci XI Sureform 60 reload, 60 mm Green 6- Row, 4.6 mm The firm became aware of a manufacturing variation in which black and green reloads in select Stapler Reloads may not deploy individual adjacent staples, which… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedMay 13, 2020ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall daVinci XI Sureform 60 Reload, 60 mm black 6-Row 4.6 mm The firm became aware of a manufacturing variation in which black and green reloads in select Stapler Reloads may not deploy individual adjacent staples, which… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 45 states named PublishedMay 13, 2020ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall 3.5mm Aresenal Screw Drill Bit Labeling Error; specifically, drill bits from lots # TSL008495A are marked with the lot # of TSL008495. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and California named
- Medical device recall ARCHITECT C Peptide Reagent - Product Usage: used as an aid in the diagnosis and treatment of patients with… Error in the renewal documentation process for license in Mexico. Class IIIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 13, 2020ClassClass IIIStatusTerminatedWhereNo state named
- Medical device recall ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients… Error in the renewal documentation process for license in Mexico. Class IIIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 13, 2020ClassClass IIIStatusTerminatedWhereNo state named
- Medical device recall ARCHITECT C Peptide Calibrator - Product Usage: used as an aid in the diagnosis and treatment of patients… Error in the renewal documentation process for license in Mexico. Class IIIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 13, 2020ClassClass IIIStatusTerminatedWhereNo state named
- Medical device recall da Vinci Xi Surgical System, IS4000 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of… Failure of Universal Surgical Manipulators due to a high friction points, resulting in an increase of arm movement to include: feelings of resistance,… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Massachusetts, Michigan, Mississippi, New York, Ohio, Pennsylvania, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall da Vinci X Surgical System, IS4200 - Product Usage: The da Vinci Xi surgical system (IS4000) is made of three… Failure of Universal Surgical Manipulators due to a high friction points, resulting in an increase of arm movement to include: feelings of resistance,… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Massachusetts, Michigan, Mississippi, New York, Ohio, Pennsylvania, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall NUVASIVE MAGEC 2 Rod X.X mm XX mm Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 44 states named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Varian Multileaf Collimator [MLC] After a recent upgrade to the collimator software version 8.5, the firm became aware that the multi-leaf collimator leaves did not move during an arc treatment. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportNationwideFDA’s word, and 28 states named PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, District of Columbia, Delaware, Florida, Georgia, Illinois, Indiana, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia and Washington named
- Medical device recall Cortoss Bone Augmentation Material Shipments were transported outside of the required refrigerated temperature conditions. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report15 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereCalifornia, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Ohio, Pennsylvania, Texas, Utah, Virginia, Washington and Wisconsin
- Medical device recall Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder Delfi Medical Innovations Inc has discovered that tourniquets cuffs in certain lots of the VariFit Sterile Single Use Thigh Cuffs, Single Port, Single Bladder… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportOhiothe one state its words name PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereOhio
- Medical device recall DELFI SINGLE USE VARIFIT TOURNIQUET CUFF SINGLE PORT SINGLE BLADDER CONTOUR THIGH CUFF WITH MATHCING LIMP… Delfi Medical Innovations Inc has discovered that tourniquets cuffs in certain lots of the VariFit Sterile Single Use Thigh Cuffs, Single Port, Single Bladder… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement ReportOhiothe one state its words name PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereOhio
- Medical device recall Tibial Tray Nonporous A Size 2 The locking mechanism of the tibial tray exhibited a manufacturing defect in which a uniform ridge was cut along the inner wall of the “T” and “Y” junctions,… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report6 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusOngoingWhereCalifornia, Florida, Ohio, Pennsylvania, Texas and Utah
- Medical device recall Tibial Tray Nonporous A Size 4 The locking mechanism of the tibial tray exhibited a manufacturing defect in which a uniform ridge was cut along the inner wall of the “T” and “Y” junctions,… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report6 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusOngoingWhereCalifornia, Florida, Ohio, Pennsylvania, Texas and Utah
- Medical device recall Visualase Cooled Laser Applicator System Tubing Set kits Product numbers: VCLAS 9735559, 3mm tip/1.65mm… The firm received complaints on the saline tubing of Visualase Cooled Laser Applicator System (VCLAS) kit, including incorrect Luer connector assembly,… Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report37 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall da Vinci SP Instrument Arm Drape The instrument drape may tear while draping the Patient Side Cart presenting a breach in the sterile barrier. Class IIFDA’s classMay 13, 2020in FDA’s Enforcement Report17 statesnamed in where it went PublishedMay 13, 2020ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Hawaii, Illinois, Maryland, Minnesota, North Carolina, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas and Virginia
Nothing matches all of these.
Remove a filter to see more. Each one is a fact FDA’s record publishes, so a recall can be left out because its record is silent on it.
Source:
FDA, Device recall enforcement reports. Released Nov 3, 2026. Updated weekly.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.”
Your shortlist0 of 4
Add one more to compare.