Medical devices, 2019
Shortlist up to four to read them side by side.
2,801 medical device recalls FDA’s Enforcement Report published in 2019, 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.
2,801of 2,801 medical device recallsshown with your filters
The list
- Medical device recall Siemens Artis Q zeego ---Interventional Fluoroscopic X-Ray System Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Siemens Artis Q.zen floor----Interventional Fluoroscopic X-Ray System Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Siemens Artis Q.zen ceiling-Interventional Fluoroscopic X-Ray System Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Siemens Artis Q.zen biplane-Interventional Fluoroscopic X-Ray System Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Siemens Artis pheno-Interventional Fluoroscopic X-Ray System Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall EVOLIS Microplate System (Catalog no. 89700) with TimeLiner Data Management Software, (Catalog no. 90471A. User-induced circumstances can contribute to the EVOLIS Microplate Processor System not handling repeat testing requests/results properly and may contribute to… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 10, 2019ClassClass IIStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall EliA RF IgM Well Potential for reporting low assay results Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Michigan, New Jersey, New York, Puerto Rico, Texas and West Virginia named
- Medical device recall REVACLEAR 300 Dialyzer There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall REVACLEAR 400 Dialyzer There is a potential presence of ruptured dialyzer fibers which may lead to a blood leak during treatment. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging… There is the possibility of viewing studies directly from the Enterprise Archive or VNA with incorrect patient images because the updated series or study is… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Florida, Georgia, Illinois, Indiana, Louisiana, Massachusetts, Missouri, New Jersey, New York, Oregon, Pennsylvania, South Carolina, South Dakota, Texas and Washington named
- Medical device recall Centricity PACS Foundation Centricity PACS software product is intended for the storage, reading, diagnostic… There is the possibility of viewing studies directly from the Enterprise Archive or VNA with incorrect patient images because the updated series or study is… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Florida, Georgia, Illinois, Indiana, Louisiana, Massachusetts, Missouri, New Jersey, New York, Oregon, Pennsylvania, South Carolina, South Dakota, Texas and Washington named
- Medical device recall ADVIA Chemistry Creatine Kinase (CK_L) reagent A steady upward trend in blank (u) absorbance was observed Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Atellica CH Creatine Kinase (CK_L) Reagent A steady upward trend in blank (u) absorbance was observed Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall SOMATOM go.Up (Model #11061610) with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1 The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, South Carolina, Texas, Virginia, Washington and Wisconsin named
- Medical device recall SOMATOM go.Now (Model #11061620), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1 The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, South Carolina, Texas, Virginia, Washington and Wisconsin named
- Medical device recall SOMATOM go.All (Model #11061630), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1 The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, South Carolina, Texas, Virginia, Washington and Wisconsin named
- Medical device recall SOMATOM go.Top (Model #1161640), with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1 The potential sporadic performance problems may result in scanning workflow interruptions and unexpected user notifications. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New York, Ohio, Pennsylvania, Puerto Rico, South Carolina, Texas, Virginia, Washington and Wisconsin named
- Medical device recall SOMATOM go.Up The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New York, Ohio, Oklahoma, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall SOMATOM go.Now The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New York, Ohio, Oklahoma, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall SOMATOM go.All The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New York, Ohio, Oklahoma, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall SOMATOM go.Top The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need… Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Michigan, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New York, Ohio, Oklahoma, South Dakota, Tennessee, Texas, Virginia and Wisconsin named
- Medical device recall Draco Enzymatic Deep-Cleaning Pad with Ready-to-Use Enzymatic Detergent, Product Number HY0305Z This product has been contaminated with Stenotrophomonas lactiubi. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement Report13 statesnamed in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereArizona, California, Florida, Iowa, Illinois, Indiana, Massachusetts, Maryland, Missouri, Pennsylvania, Tennessee, Texas and Washington
- Medical device recall First Step Draco Pad, Product Number EP-4D This product has been contaminated with Stenotrophomonas lactiubi. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement Report13 statesnamed in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereArizona, California, Florida, Iowa, Illinois, Indiana, Massachusetts, Maryland, Missouri, Pennsylvania, Tennessee, Texas and Washington
- Medical device recall CLEO Patient Monitor /Tranquility VS Patient Monitor The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the United States did not include the temperature monitor accessory option. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 10 states named PublishedJul 10, 2019ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Georgia, Louisiana, Maryland, Minnesota, Puerto Rico, South Carolina, Virginia and Wisconsin named
- Medical device recall cobas p 501 post-analytical units There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument. Class IIIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedJul 10, 2019ClassClass IIIStatusTerminatedWhereNationwide, and Alabama, California, Florida, Iowa, Illinois, Kentucky, Maryland, Oregon and Pennsylvania named
- Medical device recall cobas p 701 post-analytical units There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument. Class IIIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedJul 10, 2019ClassClass IIIStatusTerminatedWhereNationwide, and Alabama, California, Florida, Iowa, Illinois, Kentucky, Maryland, Oregon and Pennsylvania named
- Medical device recall Vereos PET/CT The Vereos PET/CT may have misaligned front and rear covers, which may result in gaps between cover parts and/or protrusion of the cover into the bore diameter. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and California, Georgia, Louisiana, Maryland, Michigan, Minnesota, Missouri, Nebraska, New Jersey, New York, Ohio, Tennessee, Texas, Vermont and Wisconsin named
- Medical device recall RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayPlan 1… When calculating electron Monte Carlo dose with a very large number of histories, the dose calculation may be wrong Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate… There is a potential for the device to fail to deliver energy to the patient. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and B1-700-00028-XXX (where XXX indicates the… The 0-arm 1000 Imaging System uses energy from the batteries to generate X-rays and move the system. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VITROS 250 Chemistry System Potential negative drift in Creatine Kinase (CK) results when used on the VITROS 250 and 350 Systems. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VITROS 250AT Chemistry System Potential negative drift in Creatine Kinase (CK) results when used on the VITROS 250 and 350 Systems. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VITROS 250 Chemistry System Refurbished Potential negative drift in Creatine Kinase (CK) results when used on the VITROS 250 and 350 Systems. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall VITROS 350 Chemistry System Potential negative drift in Creatine Kinase (CK) results when used on the VITROS 250 and 350 Systems. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall iChem VELOCITY Urine Chemistry Strips Falsely elevated (false positive) urobilinogen patient results due to an increase in the sensitivity of the urobilinogen reaction. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Powerheart¿ G5 Automatic AED Sub-supplier s documentation for specific Printed Circuit Boards (PCB) is insufficient to determine if the devices conform to specifications. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement Report3 statesnamed in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereGeorgia, Texas and Wisconsin
- Medical device recall ZOLL Pro-padz Liquid Gel Radiolucent Some of the electrodes may have been assembled incorrectly, preventing delivery of defibrillation or pacing therapy. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement Report13 statesnamed in where it went PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereArizona, California, Colorado, Connecticut, Florida, Louisiana, Minnesota, Nevada, Ohio, Pennsylvania, Tennessee, Utah and Wyoming
- Medical device recall DVR Crosslock ePAK Screw Driver There is a potential for weak seals of the sterile packaging. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 35 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin and West Virginia named
- Medical device recall DVR Crosslock ePAK Depth Gauge There is a potential for weak seals of the sterile packaging. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 35 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin and West Virginia named
- Medical device recall K-Wire Trochar Tip There is a potential for weak seals of the sterile packaging. Class IIFDA’s classJul 10, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 35 states named PublishedJul 10, 2019ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Washington, Wisconsin and West Virginia named
- Medical device recall SmartSite Syringe Administration Set-Product Package Size 50 Leaking of the Smartsite Syringe Administration Set. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJul 3, 2019ClassClass IStatusTerminatedWhereNationwide, and Arkansas, North Carolina and New Hampshire named
- Medical device recall enFlow Disposable Cartridge, used for intravenous warming therapy with fluid and blood solutions. Testing has demonstrated aluminum elution from the enFlow Disposable Cartridge during fluid warming. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IStatusTerminatedWhereNationwide
- Medical device recall enFlow Disposable Cartridge with IV Extension Set, used for intravenous warming therapy with fluid and blood… Testing has demonstrated aluminum elution from the enFlow Disposable Cartridge during fluid warming. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IStatusTerminatedWhereNationwide
- Medical device recall TASE 400 Imaging systems the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated. Class IIFDA’s classJul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IIStatusOngoingWhereNationwide
- Medical device recall TASE 500 Imaging systems the Nominal Ocular Hazard Distance (NOHD) associated with a Class lllb alignment laser utilized in its TASE family of imaging systems has been miscalculated. Class IIFDA’s classJul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose… Gas springs not always replaced within the interval specified. Class IIFDA’s classJul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 3, 2019ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Connecticut, Kansas, North Carolina, New Jersey, Oregon, Rhode Island, Tennessee, Texas and Virginia named
- Medical device recall Maquet VOLISTA StandOP Surgical Lights Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field… Class IIFDA’s classJul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Maquet VOLISTA StandOP Surgical Lights Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field… Class IIFDA’s classJul 3, 2019in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 3, 2019ClassClass IIStatusTerminatedWhereNationwide
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.”
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