Medical devices
Shortlist up to four to read them side by side.
2,589 medical device recalls FDA’s Enforcement Report published in 2026, the newest year, 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.
2,589of 2,589 medical device recallsshown with your filters
The list
- Medical device recall MEDLINE ANTERIOR HIP, Medline Kit Medline Industries, LP is issuing a recall for specific Medline kits containing B. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 29, 2026in FDA’s Enforcement Report8 statesnamed in where it went PublishedJul 29, 2026ClassClass IStatusOngoingWhereArizona, California, Florida, Illinois, Indiana, New Jersey, Ohio and South Carolina
- Medical device recall MEDLINE convenience kits labeled as: 1) C-SECTION, Medline Medline Industries, LP is issuing a recall for specific Medline kits containing B. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 29, 2026in FDA’s Enforcement Report8 statesnamed in where it went PublishedJul 29, 2026ClassClass IStatusOngoingWhereArizona, California, Florida, Illinois, Indiana, New Jersey, Ohio and South Carolina
- Medical device recall MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit Medline Industries, LP is issuing a recall for specific Medline kits containing B. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 29, 2026in FDA’s Enforcement Report8 statesnamed in where it went PublishedJul 29, 2026ClassClass IStatusOngoingWhereArizona, California, Florida, Illinois, Indiana, New Jersey, Ohio and South Carolina
- Medical device recall FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401 Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall FARASTAR Pulsed Field Ablation Generator, Product ID M004PFCE61M401 Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall FARASTAR PFA Generator, Product ID M004PFCE61M460 Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall FARASTAR Ablation Generator EU, Pulsed Field Ablation Generator, Product ID 61M401 Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNot namedno state, in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNo state named
- Medical device recall FARADRIVE Steerable Sheath Clear IDE, used to facilitate access to the vasculature and into the chambers of… Boston Scientific’s complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the… Boston Scientific’s complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall FARADRIVE STEERABLE SHEATH (CLEAR) - US, used to facilitate access to the vasculature and into the chambers… Boston Scientific’s complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall FARADRIVE STEERABLE SHEATH CLEAR OUS, used to facilitate access to the vasculature and into the chambers of… Boston Scientific’s complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall P28 PHANTON INTRAMEDULLARY NAIL SYSTEM, Phantom Hindfoot TTC/TC Ball Tipped Guide Rod, SIZE: 0.30 mm, LENGTH:… Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Hotline Fluid Warming Set, single use device, is designed to warm blood and intravenous fluids and deliver… ICU Medical became aware of an increased likelihood of leakage in specific Lots of L-70 HOTLINE Fluid Warming Sets due to potentially inadequate solvent… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Power F2 Powered Fastening System, Product No. 0567091 Powered fastening system intended for professional use… Product may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 33 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Maryland, Maine, Minnesota, Missouri, Montana, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Olympus 4K UHD LCD Monitor Potential for the HDMI and DisplayPort (DP) connectors can become faulty resulting in image loss or image abnormalities. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, New Jersey and Ohio named
- Medical device recall SeaSpine Polyaxial Head Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 25 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arizona, California, Colorado, Connecticut, Florida, Illinois, Indiana, Kansas, Maryland, Michigan, Missouri, Mississippi, Montana, Nevada, Ohio, Oklahoma, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington and Wyoming named
- Medical device recall Halyard EYE PACK Incorrect concentration of Betadine solution contained within certain AVID convenience kits. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California named
- Medical device recall MEDLINE medical procedure convenience kit labeled as: HIP CDS-LF, Medline kit The procedure kits contain ICU Medical, Inc. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 29, 2026in FDA’s Enforcement Report2 statesnamed in where it went PublishedJul 29, 2026ClassClass IStatusOngoingWhereColorado and Illinois
- Medical device recall MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit The procedure kits contain ICU Medical, Inc. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 29, 2026in FDA’s Enforcement Report2 statesnamed in where it went PublishedJul 29, 2026ClassClass IStatusOngoingWhereColorado and Illinois
- Medical device recall 3mensio Workstation (Vascular Fenestrated) software User measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to 34.4%) than… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Michigan, Minnesota, New York and Texas named
- Medical device recall Ventriculostomy Kit Ventriculostomy devices, used during ventriculostomy procedures to gain access to the ventricular system, may exhibit endotoxin levels that exceed the… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 10 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, California, Georgia, Illinois, Kentucky, Louisiana, North Carolina, Oklahoma and Utah named
- Medical device recall Brand Name: Silent Nite Product Name: Silent Nite Sleep Appliance Due to device not having FDA Clearance Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Arizona, California, Florida, Georgia, Illinois, Indiana, Maryland, Missouri, New York, Texas and Virginia named
- Medical device recall Penumbra System RED 68 Reperfusion Catheter Due to manufacturing issues, reperfusion catheters may fractures Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 37 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alaska, Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Boston Scientific TheraSphere 360 Y-90 Management Platform Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 26 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Louisiana, Massachusetts, Minnesota, Nebraska, New York, Ohio, Oklahoma, Oregon, South Carolina, South Dakota, Tennessee, Texas, Utah, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Halyard STANDARD LINE INSERTION PACK Defects in the silicone seal, which may result in “doming” of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California named
- Medical device recall Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Connecticut, Delaware, Indiana, Massachusetts, North Carolina, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Texas, Virginia and Washington named
- Medical device recall Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 20 mm 027 Incorrect labeling - embolization devices labeled as 3.0 mm x 20 mm implants contain 12 mm implants, and devices labeled as 3.0 mm x 12 mm implants contain 20… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Connecticut, Delaware, Indiana, Massachusetts, North Carolina, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Texas, Virginia and Washington named
- Medical device recall SnapshotGLO Wound Imaging Device The software controlling the wound imaging device’s battery charging circuit was not designed to recognize and recover a battery that has fully discharged into… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Nevada, Pennsylvania, Tennessee, Texas and Utah named
- Medical device recall Olympus High Flow Insufflation Unit - UHI-4 Potential for unexpected instances where the front panel display turns off unexpectedly, and air delivery (insufflation) ceases. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Emano Flow with software version v2.0.0 GS1 GTIN code: 199874903484 Emano Flow is a smartphone-based acoustic… Problem description/Reason for recall: During the period March 22, 2026, to May 29, 2026, recorded urination audio was captured at 48,000 Hz while the model… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Arkansas, Arizona, California, Colorado, Florida, Iowa, Idaho, North Carolina, New Jersey, Pennsylvania, Texas and Wisconsin named
- Medical device recall MiniMed Go App For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the associated… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 39 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons Affected kits contain recalled Bard Silastic Foley Catheters. Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Maryland, Pennsylvania and Texas named
- Medical device recall Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES, Medline Kit Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement Report10 statesnamed in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereConnecticut, Florida, Kansas, Massachusetts, Maryland, Montana, New York, Ohio, Oregon and Virginia
- Medical device recall Medline medical convenience kits labeled as: 1) SHOULDER PACK, Medline Kit Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement Report10 statesnamed in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereConnecticut, Florida, Kansas, Massachusetts, Maryland, Montana, New York, Ohio, Oregon and Virginia
- Medical device recall Medline medical convenience kits labeled as: NEURO PACK, Medline Kit Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement Report10 statesnamed in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereConnecticut, Florida, Kansas, Massachusetts, Maryland, Montana, New York, Ohio, Oregon and Virginia
- Medical device recall Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement Report10 statesnamed in where it went PublishedJul 29, 2026ClassClass IIStatusOngoingWhereConnecticut, Florida, Kansas, Massachusetts, Maryland, Montana, New York, Ohio, Oregon and Virginia
- Medical device recall SafeOp Patient Interface Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and Indiana, Missouri and Texas named
- Medical device recall Flexible Hystero-Fiberscope Kits Flexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal for… Class IIFDA’s classJul 29, 2026in FDA’s Enforcement ReportNationwideFDA’s word, and 15 states named PublishedJul 29, 2026ClassClass IIStatusOngoingWhereNationwide, and California, Florida, Georgia, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, New York, Ohio, Pennsylvania, Texas, Virginia, Vermont and Wisconsin named
- Medical device recall Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion… Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 22, 2026in FDA’s Enforcement ReportMassachusettsthe one state its words name PublishedJul 22, 2026ClassClass IStatusOngoingWhereMassachusetts
- Medical device recall Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion… Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub… FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 22, 2026in FDA’s Enforcement ReportMassachusettsthe one state its words name PublishedJul 22, 2026ClassClass IStatusOngoingWhereMassachusetts
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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