Medical devices, 2014
Shortlist up to four to read them side by side.
3,059 medical device recalls FDA’s Enforcement Report published in 2014, 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 7, 2026.
3,059of 3,059 medical device recallsshown with your filters
The list
- Medical device recall TopCare Clifford THE BIG RED DOG power toothbrush for kids! Ranir, LLC is recalling all lots of Up & Up brand Kid’s Power Toothbrush and TopCare brand Clifford Kids Power Toothbrush because the tufted disk may become… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereIllinois and Minnesota
- Medical device recall UP & UP kids’ power toothbrush Ranir, LLC is recalling all lots of UP & UP brand Kid’s Power Toothbrush and TopCare brand Clifford Kids Power Toothbrush because the tufted disk may become… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereIllinois and Minnesota
- Medical device recall Zimmer Segmental Systems After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Zimmer Segmental Systems After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems The recalling firm determined that visual inspections of the fork joints behind the detector that are conducted during six month preventive maintenance (PM)… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 40 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution In a very rare occurrence an intended movement of the SimView NT simulation system components could not be stopped with usual hand control or the collision… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report7 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereCalifornia, Kentucky, Louisiana, Massachusetts, Michigan, New York and Pennsylvania
- Medical device recall PRIMUS, ONCOR, ARTISTE Linac systems with component 550 TxT Treatment Table Update to correct the possibility for patients or operators to have their fingers trapped or pinched between the table top and the bottom frame of the 550 TxT… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Incorrect instructions for use (IFU). FDA Class I, its most serious class Class IFDA’s class (needs attention)Jan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g tube of n-BCA, one 10 mL vial of… Incorrect instructions for use (IFU). FDA Class I, its most serious class Class IFDA’s class (needs attention)Jan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall BD GeneOhm Cdiff Assay, Part #441401, containing Lysis Kit sample buffer tubes, 200 tests/kit An incorrect reagent was packed with an in vitro diagnostic kit, which may cause an increase in unresolved results or false negative results for Clostridium… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report10 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereCalifornia, Indiana, Massachusetts, Minnesota, New Jersey, New York, Ohio, Pennsylvania, South Dakota and Utah
- Medical device recall Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B Cartridges may contain individual discs which were not impregnated with antibiotic. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Oxoid Antimicrobial Susceptibility Test Discs, Norfloxacin 10 mcg., CT0434B Cartridges may contain individual discs which were not impregnated with antibiotic. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B Cartridges may contain individual discs which were not impregnated with antibiotic. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B Cartridges may contain individual discs which were not impregnated with antibiotic. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main… Carestream Health Inc. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Illinois, Indiana, Maryland, Michigan, Minnesota, North Carolina, North Dakota, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall DRX-Evolution with CSH WS These products are permanently installed diagnostic x-ray systems composed of 4… Carestream Health Inc. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Illinois, Indiana, Maryland, Michigan, Minnesota, North Carolina, North Dakota, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall DR 7500 with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main… Carestream Health Inc. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 23 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Florida, Georgia, Illinois, Indiana, Maryland, Michigan, Minnesota, North Carolina, North Dakota, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS… Carl Zeiss Microscopy, LLC has recalled the Compensator Slider Lamda 6x20 component utilized on Standard Pathology Microscopes due to misalignment of the… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Florida, Massachusetts, Maine, Michigan, North Carolina, New York and Texas named
- Medical device recall Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems An overflow flag //// is displayed in the result column for a test when the algorithm for the test cannot calculate a result or when the concentration cannot… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Brilliance CT Big Bore Radiology) Machine Name in TumorLOC Basic Mode is obscured. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Maryland, New Hampshire, Nevada, Ohio and Oregon named
- Medical device recall Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion Scales adhered to the product may be misaligned from the zero reference such that one side will not match the other. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 28 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Kansas, Massachusetts, Maryland, Michigan, Minnesota, Montana, North Carolina, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cushion Scales adhered to the product may be misaligned from the zero reference such that one side will not match the other. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 28 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Kansas, Massachusetts, Maryland, Michigan, Minnesota, Montana, North Carolina, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: Precision… Missing screws in the overhead Video Monitor Suspension. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia, Guam and Puerto Rico named
- Medical device recall ORCHESTRA/ORCHESTRA PLUS Programmer Sorin has voluntarily issued a notification to physicians related to the overestimation of the residual longevity displayed by its programmer (ORCHESTRA or… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall GE Healthcare, Dash 3000, Dash 4000 and Dash 5000 Intermittent noise on ECG and/or Respiration waveforms associated with movement of the ECG cable connector on the DASH, PDM, and/or Tram Module. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data… Intermittent noise on ECG and/or Respiration waveforms associated with movement of the ECG cable connector on the DASH, PDM, and/or Tram Module. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall GE Healthcare, TRAM MODULE, High-acuity patient monitoring Intermittent noise on ECG and/or Respiration waveforms associated with movement of the ECG cable connector on the DASH, PDM, and/or Tram Module. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Puerto Rico named
- Medical device recall Pulmonary Hemi-Artery SG Used in heart surgery Serological testing for the donor was performed with a blood sample that may have been hemodiluted due to the administration of normal saline to the donor… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportCaliforniathe one state its words name PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereCalifornia
- Medical device recall Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within… The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected shutdown of the system while in use,… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an ophthalmic surgical laser indicated for use in the… A defect in the controller board can lead to the condenser to the video monitor becoming too warm. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Illinois and New Jersey named
- Medical device recall Vital Signs Anesthesia Circuits The Ventilator Circuit is intended for use as an interface between a… A circuit in use was occluded by a blue port cap that was inadvertently attached to the circuit as a result of an internal inspection error and will cause… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular administration set. Defective component may cause extension sets to leak. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Delaware, Florida, Illinois, Missouri, New York, Ohio, Oregon and Virginia named
- Medical device recall MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Catheter Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter because a small number of Silicone catheters in the may be… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Titanium Single Lumen Low-Profile port, with Pre-Attached open-Ended Silicone 6.6Fr Catheter Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter because a small number of Silicone catheters in the may be… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer… RADIOMETER become aware that if the ABL90 FLEX is tilted, this may potentially cause a negative bias on sodium (Na+) results. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report41 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia
- Medical device recall VITROS Chemistry Products COCM Reagent Inaccurate quality control results. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 34 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Virginia, Washington and Wisconsin named
- Medical device recall Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative… Complaints were received regarding variability in recovery of QC and patient results with certain lots of the Dimension Vista CSA Flex reagent cartridges. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Composix L/P with Echo PS 10” X 13” Product labeling does not match product configuration. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 14 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Georgia, Iowa, Illinois, Indiana, Missouri, Nebraska, New Mexico, New York, Ohio, Pennsylvania, Texas and Virginia named
- Medical device recall Composix L/P with Echo PS 6” X 8” Product labeling does not match product configuration. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 14 states named PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Georgia, Iowa, Illinois, Indiana, Missouri, Nebraska, New Mexico, New York, Ohio, Pennsylvania, Texas and Virginia named
- Medical device recall Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of… Covidien is correcting labeling to clarify the operational life of the oxygen sensor (O2 sensor), PN 4-072214-00 used in the Puritan Bennett” 840, and PN,… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series Operators Manual: PN 10066984 & PN… Covidien is correcting labeling to clarify the operational life of the oxygen sensor (O2 sensor), PN 4-072214-00 used in the Puritan Bennett” 840, and PN,… Class IIFDA’s classJan 29, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Siemens CentraLink” Data Management System V14.0.4, V14.0.5 or V14.0.8 The CentraLink system software is a… Under extremely rare circumstances, a patient result that had been previously disabled may be released without proper review. Class IIFDA’s classJan 29, 2014in FDA’s Enforcement Report3 statesnamed in where it went PublishedJan 29, 2014ClassClass IIStatusTerminatedWhereMinnesota, New Jersey and Nevada
- Medical device recall King Systems KLTSD414 Quantity, 5 PER CASE KING LTSD KIT SIZE 4 King LT(S)-DTM supraglottic airway… KLTD214 airways found inside KLTSD414 packages. Class IIFDA’s classJan 22, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereCalifornia and New York
- Medical device recall Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 9-12 mm Injects Above UPN: M00547100 The… Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size Class IIFDA’s classJan 22, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm Injects Above UPN: M00547110 Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size Class IIFDA’s classJan 22, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm Injects Below UPN :M00547140 Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size Class IIFDA’s classJan 22, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall pO2 D999 membrane units RADIOMETER became aware that the regarded lot pO2 units 942-042R0971 were produced with inner solution for pCO2 membrane units. Class IIFDA’s classJan 22, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereNationwide, and Colorado, Connecticut, Georgia, Massachusetts, Missouri and Mississippi named
- Medical device recall Draeger Infinity Acute Care System Monitoring Solution After a test in which a low SpO2 (yellow) medium grade alarm initiated in neo-natal mode and was subsequently paused, the high grade life threatening SpO2… Class IIFDA’s classJan 22, 2014in FDA’s Enforcement Report8 statesnamed in where it went PublishedJan 22, 2014ClassClass IIStatusTerminatedWhereCalifornia, Illinois, Indiana, Massachusetts, New Hampshire, New York, Oklahoma and Texas
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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