Medical devices, 2024
Shortlist up to four to read them side by side.
3,394 medical device recalls FDA’s Enforcement Report published in 2024, 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.
3,394of 3,394 medical device recallsshown with your filters
The list
- Medical device recall Medline Kits, trays, and packs labeled as follows: a) KIT,SUCTION CATH,10FR W/WATER Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: MAINTENANCE FLUSH KIT/BLOOD DRAW Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: a) DIALYSIS ACCESSORY PACK W/O CATHETER Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: EYE PREP KIT Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: a) BASIC PROCEDURE TRAY Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: LATEX FREE TRACHEOSTOMY CARE TRAY Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: a) IV SECUREMENT KIT Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: LACERATION TRAY Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: a) A C DAILY WET KIT Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: BREAST BIOPSY KIT Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Centurion Kits, trays, and packs labeled as follows: CIRCUMCISION TRAY Medline Industries, LP is recalling certain kits and trays that were manufactured using specific lots of Nurse Assist (as components): 0.9% Sodium Chloride… FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and Puerto Rico named
- Medical device recall Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites Potential for catheter disconnection from the patient line stopcock connectors. FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and 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, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Medtronic Duet External Drainage and Monitoring System, SmartSite, Injection Sites Potential for catheter disconnection from the patient line stopcock connectors. FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and 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, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter Potential for catheter disconnection from the patient line stopcock connectors. FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and 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, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Catheter Potential for catheter disconnection from the patient line stopcock connectors. FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and 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, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter Potential for catheter disconnection from the patient line stopcock connectors. FDA Class I, its most serious class Class IFDA’s class (needs attention)Mar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 50 states named PublishedMar 6, 2024ClassClass IStatusOngoingWhereNationwide, and 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, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall IdentiTi ALIF Standalone Interbody System Due to reports of intraoperative graft bolt implantation breakages. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 32 states named PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide, and Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Iowa, Idaho, Indiana, Kansas, Kentucky, Maryland, Michigan, Minnesota, Mississippi, North Carolina, New Hampshire, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Washington and Wisconsin named
- Medical device recall Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide intravenous infusion of parenteral fluids,… When utlizing the patient query feature on the Zyno Medical Z-800WF pumps with software version 5.2.05, the alarm volume may inadvertently revert from a higher… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Rebstock Holding rod for fixation -For holding and fixation of flexible Leyla Arms and spatula Art Holding arm could move (twist) uncontrollably in the front area. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportTexasthe one state its words name PublishedMar 6, 2024ClassClass IIStatusOngoingWhereTexas
- Medical device recall Schiff Reagent, Hotchkiss-McManus This IVD is colorless. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement Report8 statesnamed in where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereAlabama, Illinois, Massachusetts, Minnesota, New Jersey, Pennsylvania, Texas and Virginia
- Medical device recall In-vitro diagnostic kits Products that were intended for export only which were not approved or registered in accordance with U.S. Class IIIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedMar 6, 2024ClassClass IIIStatusOngoingWhereNationwide, and Alabama, California, Illinois, Massachusetts, Maryland, Minnesota, New York and Pennsylvania named
- Medical device recall In-vitro diagnostic kits Products that were intended for export only which were not approved or registered in accordance with U.S. Class IIIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedMar 6, 2024ClassClass IIIStatusOngoingWhereNationwide, and Alabama, California, Illinois, Massachusetts, Maryland, Minnesota, New York and Pennsylvania named
- Medical device recall Wash station: M1000 Wash Station Assembly & DITI Slide Products that were intended for export only which were not approved or registered in accordance with U.S. Class IIIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedMar 6, 2024ClassClass IIIStatusOngoingWhereNationwide, and Alabama, California, Illinois, Massachusetts, Maryland, Minnesota, New York and Pennsylvania named
- Medical device recall NxStage Cartridge Express with Speedswap Product is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement Report19 statesnamed in where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereArizona, California, Colorado, Georgia, Illinois, Indiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Jersey, New York, Tennessee, Texas, Virginia and Wisconsin
- Medical device recall GRAPHENANO DENTAL G-CAM Machining error on cams renders the device unusable. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide, and Utah named
- Medical device recall Ref No: 31156 / COMBO KIT CONTAINS INS-8301, INS-4500,INS-HITH A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: HITHSP04 / Integra Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: HITHSP06 / Integra Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INS5HND / Integra Cranial access kit (without Prep solutions) Bit and Guard A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INS7250 / Integra Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INS7260 / Integra¿ Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INS7270 / Integra¿ Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall INS7280 / Integra¿ Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INSHITH / Integra¿ Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INSHITHND / Integra¿ Cranial access kit (without Prep solutions) Bit and Guard A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Ref No: INSHITHRZN / Integra Cranial Access Kit A defect in the sterile packaging (header bag) of the Cranial Access Kit failing the required packaging integrity testing criteria. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Tensive Conductive Adhesive Gel, Product Ref. 22-60. 12, 1 case contains 12 inner boxes with 50g tubes Five complaints were received related to viscosity of Tensive Conductive Adhesive Gel Ref 22-60. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement Report10 statesnamed in where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereArizona, California, Florida, North Carolina, New Jersey, Nevada, New York, Pennsylvania, Washington and Wisconsin
- Medical device recall Colonoscope, Model Number CF-H180AL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number CF-HQ190I. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number CF-HQ190L. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number CF-Q180AL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-H180AL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-H190DL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-H190L. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-H190TL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-HQ190L. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall Colonoscope, Model Number PCF-Q180AL. Specific repaired colonovideoscopes were assembled without an adhesive which protects them from certain physical conditions such as high levels of vibration,… Class IIFDA’s classMar 6, 2024in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereNationwide
- Medical device recall USTAR II Hip System Press-Fit Curved Stem, RHS Ti Plasma Spray for the following reference numbers Their is a potential that the implant curved stem may be oriented incorrectly. Class IIFDA’s classMar 6, 2024in FDA’s Enforcement Report9 statesnamed in where it went PublishedMar 6, 2024ClassClass IIStatusOngoingWhereCalifornia, Colorado, Florida, Indiana, Kentucky, Michigan, Nevada, Tennessee 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.”
Your shortlist0 of 4
Add one more to compare.