Medical devices, 2012
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1,310 medical device recalls FDA’s Enforcement Report published in 2012, 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.
1,310of 1,310 medical device recallsshown with your filters
The list
- Medical device recall Vygon VY(TM)Flush Heparin Lock Flush Syringes, 1 Unit per mL, 3mL in a 10mL Flush Syringe, 30 syringes per… Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per… Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per… Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per… Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Vygon VY(TM)Flush Heparin Lock Flush Syringes, 100 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per… Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Churchill Medical Systems, Inc Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Iowa, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Pennsylvania, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall T5 Hytrel Zipper Toga The clear tape, that is intended to aid in the prevention of patients fluids from contacting the surgeon/surgical staff through the sleeve seam of the toga,… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 39 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall T4-Hytrel Zipper Toga Product Usage - The togas are intended to provide a barrier between the operating room… The clear tape, that is intended to aid in the prevention of patients fluids from contacting the surgeon/surgical staff through the sleeve seam of the toga,… Class IIFDA’s classJun 20, 2012in FDA’s Enforcement ReportNationwideFDA’s word, and 39 states named PublishedJun 20, 2012ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, 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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