Medical devices, 2023
Shortlist up to four to read them side by side.
2,477 medical device recalls FDA’s Enforcement Report published in 2023, 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.
2,477of 2,477 medical device recallsshown with your filters
The list
- Medical device recall Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold) 20 TESTS/1… Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market approval, clearance or Emergency Use Authorization. FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide, and California and Texas named
- Medical device recall CADD Administration Set, List Numbers: a) There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False “No… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide
- Medical device recall CADD Administration Set, List Numbers: 1) There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False “No… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide
- Medical device recall CADD Administration Set, List Numbers: a) There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False “No… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide
- Medical device recall CADD Administration Set, List Numbers: a) There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False “No… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide
- Medical device recall CADD Administration Set, List Numbers: 1) There are two potential issues with CADD Infusion System Infusion Sets: (1) Lack of Delivery or Underdelivery related to Tubing Occlusion and (2) False “No… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IStatusOngoingWhereNationwide
- Medical device recall SynCardia Total Artificial Heart System Due to tears reported tears in the cannula due to wear and tear stress. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 28 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Florida, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, OXY/CVR COMBO BB841 FUSION… An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and… An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and… An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Non-sterile procedural trays labeled as CRANI, 2 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as LAPAROTOMY CDS, 2 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as THEDA CLARK TOTAL KNEE CDS, 1 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case Potential for sterile blades, within non-sterile SPT kits containing the blades, to puncture the outer foil layer causing a breach in the sterile packaging. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Maryland, Washington and Wisconsin named
- Medical device recall OSS Modular Arthrodesis Nail, 7 Degree Collar Assembly with Locking Bolts-For use in the replacement of… Product missing the four small locking collar bolts resulting in extension of surgery to find a replacement Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and California, Florida and Kentucky named
- Medical device recall Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized… Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and California, Iowa, Indiana, Louisiana, North Carolina, New Hampshire, New York, Ohio, South Dakota, Texas, Virginia and Wisconsin named
- Medical device recall Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized… Pod may have weld failures breaching the sterile barrier and result in the use of unsterile instruments leading to infection or other major injuries. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and California, Iowa, Indiana, Louisiana, North Carolina, New Hampshire, New York, Ohio, South Dakota, Texas, Virginia and Wisconsin named
- Medical device recall AxiEM” Non-Invasive Patient Tracker Due to increasing complaint trend for the Non-Invasive Patient Tracker system where complaints analysis indicates that users are unable to successfully verify… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement Report41 statesnamed in where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereAlabama, Arkansas, Arizona, California, Colorado, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall System Material # Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee multi-purpose 10094139 Artis… In rare cases, the system may only boot into backup mode after an abrupt shutdown and not reach full operating mode. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Mammotome MammoStar Biopsy Site Identified The label incorrectly identifies the product as STAR1401, a 1x3mm Barbell shaped marker pre-loaded in a 14 gauge needle, while the packaging contains STAR1402,… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedFeb 8, 2023ClassClass IIStatusTerminatedWhereNationwide, and Ohio named
- Medical device recall (1) Vanguard Knee System PS Open Box Femoral Components Incorrectly labeled as either smaller or larger and incorrect side (right/left). Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement Report6 statesnamed in where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereFlorida, Indiana, Maryland, Ohio, Pennsylvania and Wisconsin
- Medical device recall (1) Vanguard Knee System PS Open Box Femoral Components Incorrectly labeled as either smaller or larger and incorrect side (right/left). Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement Report6 statesnamed in where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereFlorida, Indiana, Maryland, Ohio, Pennsylvania and Wisconsin
- Medical device recall BIOPSY MEDIUM 10ML, Reference Number 10620010 A, used for blastomere biopsy of cleavage stage embryos for… The affected product may contain a medium other than the Biopsy Medium. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNo state named
- Medical device recall MEDLINE UNITE FOOT & ANKLE Screw, Non-Locking, Mini T8 The recall is due to observed intra-operative screw failure. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall MEDLINE UNITE FOOT & ANKLE Screw, Polyaxial Locking, Mini T8 The recall is due to observed intra-operative screw failure. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall MEDLINE UNITE FOOT & ANKLE DRILL BIT, 1.3MM Solid Core The recall is due to observed intra-operative screw failure. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall GORE CARDIOFORM Septal Occluder Septal Occluders released with incomplete quality test documentation that assesses the release of the device from the delivery system during the index… Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arkansas, California, Connecticut, Florida, Indiana, Massachusetts, Missouri, New York, South Dakota, Texas and Virginia named
- Medical device recall Lucid TCD 2.0 System Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which will cause the system to freeze and reboot. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arizona, Illinois, Pennsylvania, South Carolina and Texas named
- Medical device recall NovaGuide Intelligent Ultrasound System Transcranial Doppler/ultrasound system tablet has a faulty hard drive, which will cause the system to freeze and reboot. Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedFeb 8, 2023ClassClass IIStatusOngoingWhereNationwide, and Arizona, Illinois, Pennsylvania, South Carolina and Texas named
- Medical device recall Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV… Due to the adhesive provided within the catheter repair kits maybe hardened/coagulated (unusable). Class IIFDA’s classFeb 8, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 49 states named PublishedFeb 8, 2023ClassClass 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, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Getinge Flow-i Anesthesia Systems Flow-i C20 Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 20 states named PublishedFeb 1, 2023ClassClass IStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Indiana, Massachusetts, Michigan, Missouri, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington and West Virginia named
- Medical device recall Getinge Flow-c Anesthesia System Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 20 states named PublishedFeb 1, 2023ClassClass IStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Indiana, Massachusetts, Michigan, Missouri, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington and West Virginia named
- Medical device recall Getinge Flow-e Anesthesia System Due to a software bug, under certain conditions, pressure cannot be built up resulting in no ventilation. FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 20 states named PublishedFeb 1, 2023ClassClass IStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Indiana, Massachusetts, Michigan, Missouri, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington and West Virginia named
- Medical device recall Software : myNeedle Guide 2D license, myNeedle Guide 2D AWP only Workflow license, or myNeedle Guide 3D… In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order of the orientation labels head , center, and feet in the axial thick slice… Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Agfa HealthCare Enterprise Imaging XERO Viewer There is a software defect that can cause issues with images. Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Veritas Advanced Infusion Packs Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or… Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement Report8 statesnamed in where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereFlorida, Illinois, Minnesota, Mississippi, New York, Ohio, Tennessee and Texas
- Medical device recall FUSION Dual Pump Packs Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or… Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement Report8 statesnamed in where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereFlorida, Illinois, Minnesota, Mississippi, New York, Ohio, Tennessee and Texas
- Medical device recall Single-Use Packs Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or… Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement Report8 statesnamed in where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereFlorida, Illinois, Minnesota, Mississippi, New York, Ohio, Tennessee and Texas
- Medical device recall Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Leakage of the original specimen from the plastic microfluidic cartridge (PIE), possibility that laboratory personnel may be exposed to aerosolized specimen… Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Indiana, Kansas, Kentucky, Louisiana, Michigan, Minnesota, North Carolina, New York, Oregon and Texas named
- Medical device recall Alinity m System The firm identified the following three potential issues which may have impacted ADUs installed on distributed Alinity m Systems. Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNo state named
- Medical device recall Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Potential for pilot balloon non-inflation or cuff non-deflation. Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 38 states named PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Endotracheal Tube labeled as the following: a Potential for pilot balloon non-inflation or cuff non-deflation. Class IIFDA’s classFeb 1, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 38 states named PublishedFeb 1, 2023ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
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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