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 ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 6 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Colorado, Florida, Illinois, North Carolina, Pennsylvania and Texas named
- Medical device recall NavioPFSTM System, Orthopedic Sterotaxic Instrument Blue Belt Technologies is conducting a voluntary recall for their Navio PFS system which is used during orthopedic knee surgery. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report4 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereCalifornia, Ohio, Pennsylvania and Texas
- Medical device recall Enaly 1000 BT-12 Ozone Generator William Domb is recalling the Enaly 1000 BT-12 Ozone Generator because it is not approved or cleared by the FDA for medical use. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report8 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereCalifornia, Florida, Hawaii, Indiana, North Carolina, Tennessee, Texas and Washington
- Medical device recall Recalled product is a component of the Newport Medical Instruments e360 Ventilator: single board computer Reports of the audible alarm not sounding when the ventilator is in an alarm state. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report16 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereArizona, California, Colorado, Connecticut, Florida, Georgia, Kentucky, Massachusetts, Maryland, Missouri, Nevada, Pennsylvania, Rhode Island, Texas, Virginia and Washington
- Medical device recall DROP LOK” Knee Brace***LATEX FREE” Product Usage: Used in the treatment, support, and rehabilitation of many… During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 29 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Maryland, Michigan, Missouri, North Carolina, Nebraska, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Cartilage Knee Brace***LATEX FREE” Product Usage: Used in the treatment and support of many types of knee… During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 29 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Maryland, Michigan, Missouri, North Carolina, Nebraska, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Hinged Knee Support***LATEX FREE” Product Usage: Provide added lateral stability and allows the knee to… During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 29 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Maryland, Michigan, Missouri, North Carolina, Nebraska, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall Tennis Elbow Support, Neoprene***LATEX FREE” Product Usage: Provides compression and warmth for mild to… During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 29 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Maryland, Michigan, Missouri, North Carolina, Nebraska, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Utah, Virginia, Vermont, Washington, Wisconsin and West Virginia named
- Medical device recall HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a… Patients and caregivers are instructed that if a battery does not provide two hours of support or behaves unusually, that battery should no longer be used and… Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report37 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Ultrasound needles, 22G Ultrasound needles may be defective and leak at the needle hub. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereIllinois and Maryland
- Medical device recall Ultrasound USB needles, with 30 degree bevel Ultrasound needles may be defective and leak at the needle hub. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report2 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereIllinois and Maryland
- Medical device recall PS-C Femoral Nonporous Rt Sz 6 A femoral component containing pegs was found in a box for the pegless version. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Arizona and Nevada named
- Medical device recall DPM 6 Monitor in use with a Multi Parameter Module (MPM) The MPM included a cardiac ST/Arrhythmia analysis feature which is not cleared for marketing. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Ohio named
- Medical device recall Mucus Specimen Trap 40 cc, Specimen Trap 40 cc with additional transport cap There is a potential that the specified mucus specimen traps are not sterile. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and California, Massachusetts, Maryland, Michigan, Minnesota, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Texas and Utah named
- Medical device recall Syngo Dynamics v9.5 system Systems with the affected serial number are experiencing a software error which may lead to incorrect patient demographics display. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 21 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, California, Connecticut, Georgia, Iowa, Illinois, Kansas, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Washington, Wisconsin and West Virginia named
- Medical device recall Coaxial Micro-Introducer Kit Greatbatch identified that the documentation does not support the five-year shelf life of the Bard Access Division Coaxial Micro-Introducer Set. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Utah named
- Medical device recall ExploR 7x26mm Modular Radial Stem This lot of the ExploR Modular Radial Stem may be missing the wedge ramp threads. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Maryland, Michigan, North Carolina, Nevada, New York, Oregon and South Carolina named
- Medical device recall ACCU-CHEK Compact Plus Test Strips For use with: ACCU-CHEK Compact Plus Meters Roche Diabetes Care has become aware the ACCU-CHEK Compact Plus test strips may produce erroneously low blood glucose readings in patients undergoing… Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall McKesson Radiology-PACS High priority alert icon was not displayed in the Study List when there are no Stat studies present. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 21 states named PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Georgia, Iowa, Idaho, Illinois, Maryland, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, Nevada, New York, Pennsylvania, Tennessee, Texas, Vermont, Washington, West Virginia and Wyoming named
- Medical device recall Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards and also 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may fail to detect a disconnected Ultrafiltration (UF) Pump Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Revision K Actuator Test Boards 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may fail to detect a disconnected Ultrafiltration (UF) Pump Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall RAPIDFILL Syringe Strip, For use with RAPIDFILL Automated Syringe Filler (ASF): H93890200 RAPIDFILL Syringe… Possible breach in sterile barrier for inner and outer bags of the product. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement Report21 statesnamed in where it went PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Connecticut, Florida, Georgia, Hawaii, Illinois, Kansas, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, Nevada, Ohio, Oregon, Pennsylvania, Tennessee, Virginia and Wisconsin
- Medical device recall InterValve V8 Balloon Aortic Valvuloplasty Catheter Leak issues were discovered through accelerated age testing. Class IIFDA’s classMay 21, 2014in FDA’s Enforcement ReportTennesseethe one state its words name PublishedMay 21, 2014ClassClass IIStatusTerminatedWhereTennessee
- Medical device recall INOmax DSIR, model 10007, Nitric Oxide Delivery System, with Software version 3.0.0. The INOmax DS delivery… An anomaly impacts the monitoring system of INOmax DSIR Plus (software 3.0.0). Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide, and District of Columbia and Virginia named
- Medical device recall Variant II beta-thalassemia Short Program There is an issue with the buffers which impacts the quantification of the Hemoglobin F peak. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report10 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Connecticut, Georgia, Louisiana, Massachusetts, North Carolina, New Jersey, New York and Washington
- Medical device recall Joseph Lamelas Atrial Lift System The support arm attached with an adhesive to the body of the blade is detaching while attempting to engage the visor component. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportMinnesotathe one state its words name PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereMinnesota
- Medical device recall Alere Triage BNP Test for the Beckman Coulter Access Family of Immunoassay Systems These lots may not recover within range when tested using certain commercially available controls. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall RetractaBed , Clinical Contour, Med - Mizer Inc.... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall RetractaBed , Clinical Contour, Med - Mizer Inc.... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall RetractaBed , Clinical Contour, Med - Mizer Inc.... All configurations of the SS Retractabed, Clinical Contour, made prior to June 7, 2008 may have had insufficient welding on the foot cross tube. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 12-Instrument Sterilization Tray Gravity sterilization parameters provided in the 12 Instrument Sterilization reprocessing guide did not fully consider all worst-case scenarios during… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall CLINITEK Status+ Analyzer (portable urine chemistry analyzer) Device with Sample Interference Notes (SIN) enabled not cleared for US marketing. Class IIIFDA’s classMay 14, 2014in FDA’s Enforcement ReportCaliforniathe one state its words name PublishedMay 14, 2014ClassClass IIIStatusTerminatedWhereCalifornia
- Medical device recall Alere INRatio2 PT/INR Professional Test Strips Test Strips may report an inaccurately low INR result. FDA Class I, its most serious class Class IFDA’s class (needs attention)May 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IStatusTerminatedWhereNationwide
- Medical device recall Giraffe¿ Infant Warmers integrated with Nellcor SpO2 Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Panda¿ iRes Infant Warmers integrated with Nellcor SpO2 Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Panda¿ Freestanding Infant Warmers, integrated with Nellcor SpO2 Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Panda¿ Wall-Mount Infant Warmers, integrated with Nellcor SpO2 Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Nellcor SpO2 Upgrade kit, consists of a Nellcor SpO2 circuit board, an OEM part Medical device software may be defective and may cause user-set alarm limits to result in false positive or false negative Oxygen saturation and pulse rate… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNot namedno state, in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall TX1 Tissue Removal System The sterile barrier in the packaging may be compromised due to cracks in the thermoform tray that may occur during transport of the product in extreme cold… Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ADVIA Centaur XP Immunoassay system, an automated in vitro diagnostic analyzer Instrument Cover Gas Spring failures. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bausch & Lomb, Biotrue, Multi-purpose contact lens solution, 10 fl.oz., Sterile. Out of specification results for one of the two disinfectants. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Nonabsorbable Surgical Suture, U.S.P., Sterile - Do Not Resterilize, Deknatel Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Teleflex Medical, Research Triangle Park, NC, Braided Polyester Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Teleflex Medical, Research Triangle Park, NC, Polypropylene Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture,… Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Bard Fixt Suture Braided Polyester Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless Steel Suture, Nonabsorbable… Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
- Medical device recall Deknatel Teleflex Medical Silk Black Braided Silk Suture Nonabsorbable Surgical Suture U.S.P Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use. Class IIFDA’s classMay 14, 2014in FDA’s Enforcement Report28 statesnamed in where it went PublishedMay 14, 2014ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Georgia, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maine, Michigan, Minnesota, Missouri, Mississippi, New Jersey, New Mexico, Nevada, New York, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia
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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