Medical devices, 2017
Shortlist up to four to read them side by side.
2,615 medical device recalls FDA’s Enforcement Report published in 2017, 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 5, 2026.
2,615of 2,615 medical device recallsshown with your filters
The list
- Medical device recall Zimmer Natural Nail System Freehand Drill 4.3 mm Diameter 152.5 mm Length Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Drill Bit Quick-Connect 4.5 mm Diameter 145 mm Length Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Drill Bit Quick-Connect 3.2 mm Diameter 195 mm Length Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Guide Sleeve 3.25 Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall THREAD RETRIEVAL DRILL Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall ABUT GOLD FRICTION-FIT Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall TRY-IN,ABUTMENT, CONT, 3.5X4.5 Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall IMPRESSION CAP CONT 3.5MM Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall WAXING COPING, CONT 3.5 MM,ANG Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall IMPLANT,1-PC,ANG,3.0X10MM Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall IMRIS DEERFIELD IMAGING incorrect thread on thumbscrews Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report3 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereIllinois, Oregon and Pennsylvania
- Medical device recall LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c)… Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall UniPerc(R) Adjustable Flange Tracheostomy Tube kit, Reorder Number 100/897/080 CZ The UniPerc(R) Tracheostomy… Smiths Medical became aware that one lot of the 8.0mm UniPerc(R) Adjustable Flange Tracheostomy Tube kit, product reorder number 100/897/080 CZ, lot number… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Ultradent Products, Inc The barcode label was placed underneath the sterile barrier and the product was re-wrapped. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultradent Products, Inc The barcode label was placed underneath the sterile barrier and the product was re-wrapped. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultradent Products, Inc The barcode label was placed underneath the sterile barrier and the product was re-wrapped. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultradent Products, Inc The barcode label was placed underneath the sterile barrier and the product was re-wrapped. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultradent Products, Inc The barcode label was placed underneath the sterile barrier and the product was re-wrapped. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to… For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report29 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia
- Medical device recall FUJINON ED-530XT An update to the design and labeling was implemented to help reduce patient risk associated with inadequate reprocessing of the device. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR Specific lots labeled as an Antibacterial Hydrophilic Intermittent Catheter may lack the hydrophilic coating. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report23 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Missouri, North Carolina, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia and Washington
- Medical device recall Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm It was determined that the deflection length indicated on the Guide catheter handle does not match the label on the box and sterile packaging for two lots. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement Report8 statesnamed in where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereArizona, California, Florida, Georgia, Massachusetts, Michigan, Minnesota and New Hampshire
- Medical device recall Platinium VR 1210 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Platinium DR 1510 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Platinium CRT DF1 1711 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Platinium VR DF4 1240 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Platinium DR DF4 1540 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac ResynchronizationTherapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Platinium CRT-D 1741 There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators… Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall NOVADAQ SPY-PHI Drape, 7” x 104” The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Idaho, Illinois, New York, Oregon and Virginia named
- Medical device recall NOVADAQ SPY-PHI PAQ Intended for use with the SPY-PHI System The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Idaho, Illinois, New York, Oregon and Virginia named
- Medical device recall NOVADAQ SPY-PHI Drape, 7” x 104” The sterile drape material may contain a pinhole compromising its integrity resulting in a breach of the sterile barrier. Class IIFDA’s classOct 4, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 7 states named PublishedOct 4, 2017ClassClass IIStatusTerminatedWhereNationwide, and California, Colorado, Idaho, Illinois, New York, Oregon and Virginia named
- Medical device recall VITEK(R) 2 GP Customer reports have indicated occurrences of atypical negative O129R reactions for Enterococcus casseliflavus ATCC(R) 700327(TM) in association with VITEK(R)… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement ReportGuamthe one state its words name PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereGuam
- Medical device recall AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer is intended for use as an in vitro diagnostic… Beckman Coulter has identified that an incorrect setting using a proprietary software configuration tool can result in the Sample Prep Probe of the AQUIOS CL… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Euphora Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA)… Stylette removal difficulties on the Euphora and Solarice products. Class IIFDA’s classSep 27, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Solarice Rapid Exchange Balloon Dilatation Catheter, a Percutaneous Transluminal Coronary Angioplasty (PTCA)… Stylette removal difficulties on the Euphora and Solarice products. Class IIFDA’s classSep 27, 2017in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall K-Assay(R) Multi-Analyte Calibrator The AlAT calibrator values in the package insert for the Multi-Analyte Calibrator, lot D755, lots N653 and lot N654 were not correct. Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report14 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereCalifornia, Connecticut, Florida, Iowa, Illinois, Massachusetts, Maryland, North Carolina, New Jersey, New York, Ohio, Texas, Virginia and Washington
- Medical device recall Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation… Potential for Spinal Clamps to be damaged when opened beyond intended limits, either no opening once attached to a patient’s spinous process or leaving a… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report44 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Spine Referencing Instrumentation, Spinous Process Clamp, Short When used with a Medtronic StealthStation… Potential for Spinal Clamps to be damaged when opened beyond intended limits, either no opening once attached to a patient’s spinous process or leaving a… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report44 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Spine Referencing Instrumentation, Double Spinous Process Clamp, Tall When used with a Medtronic… Potential for Spinal Clamps to be damaged when opened beyond intended limits, either no opening once attached to a patient’s spinous process or leaving a… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report44 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Spine Referencing Instrumentation, Double Spinous Process Clamp, Short When used with a Medtronic… Potential for Spinal Clamps to be damaged when opened beyond intended limits, either no opening once attached to a patient’s spinous process or leaving a… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report44 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall Spine Referencing Instrumentation, Set, Contains Spinous Process Clamps, Short and Tall When used with a… Potential for Spinal Clamps to be damaged when opened beyond intended limits, either no opening once attached to a patient’s spinous process or leaving a… Class IIFDA’s classSep 27, 2017in FDA’s Enforcement Report44 statesnamed in where it went PublishedSep 27, 2017ClassClass IIStatusTerminatedWhereAlabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia and Wyoming
- Medical device recall X-Laser Laser Light Show projector models Aurora, Caliente Aurora, PSX-400, Mobile Beat Max, Mobile Beat Max… Failure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation Class IIFDA’s classSep 20, 2017in FDA’s Enforcement ReportNot namedno state, in where it went PublishedSep 20, 2017ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall Skintact Electrode for Defibrillation, Pacing, Monitoring, Cardioversion Certain lots of the defibrillation electrodes model DF59N and DF59NC may have a delay in connecting or not connect at all with the defibrillator ZOLL AED PLUS. FDA Class I, its most serious class Class IFDA’s class (needs attention)Sep 20, 2017in FDA’s Enforcement Report2 statesnamed in where it went PublishedSep 20, 2017ClassClass IStatusTerminatedWhereFlorida 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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