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All recalls Car seats760 Food29,584 Home products7,066 Kids’ products3,016 Medical devices40,450 Medicines18,075 Pets66 Reports to CPSC70,000 Tires795 Vehicle equipment2,877 Vehicles23,148

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All places9 of 13 nationwide Read from public records on Nov 6, 2026 How it works

Recalls Medical devices 2023

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

By the year FDA published them20262,589 20252,908 20243,39420232,47720222,192 20212,303 20203,055 20192,801 20183,757 20172,615 20163,246 20152,495 20143,059 20132,249 20121,310

Filters

FDA’s class Class IClass IIClass III

FDA’s own classes: Class I is the most serious. Each recall’s page quotes FDA’s definition.

Status, in FDA’s file OngoingCompletedTerminated

Where it went, in FDA’s words FDA says nationwideAlabamaAlaskaAmerican SamoaArizonaArkansasCaliforniaColoradoConnecticutDelawareDistrict of ColumbiaFloridaGeorgiaGuamHawaiiIdahoIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMississippiMissouriMontanaNebraskaNevadaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaNorth DakotaNorthern Mariana IslandsOhioOklahomaOregonPennsylvaniaPuerto RicoRhode IslandSouth CarolinaSouth DakotaTennesseeTexasUS Virgin IslandsUtahVermontVirginiaWashingtonWest VirginiaWisconsinWyoming

The states FDA’s words on where the product went name. “Nationwide” is its own choice: to FDA it means the fifty states or a significant portion, so a recall is never counted for a state its words don’t name.

The reason May fail, or give wrong resultsChemicals, metals or drugs that shouldn’t be in itSterility not assuredLabels that are wrong or missingPieces of metal, glass or plasticStrength, purity or how it was madeGerms: Listeria, Salmonella, E. coli and others

Grouped from FDA’s own reason for each recall, which every record shows in full.

Published in FDA’s report

Any

In FDA’s record Class IStill ongoing

The list

Filter by product, brand, reason or number

Order the list NewestNewest firstNameName

Medical device recallsPublishedClassStatusWhere

Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal uncuffed/plain - Murphy Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
Medical device recall RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products. FDA Class I, its most serious class Class IFDA’s class (needs attention)Jul 5, 2023in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJul 5, 2023ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named

Before these 1,249 to 1,296 of 2,477 After these

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.”

Medical devices, 2023

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