Medical devices, 2013
Shortlist up to four to read them side by side.
2,249 medical device recalls FDA’s Enforcement Report published in 2013, 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.
2,249of 2,249 medical device recallsshown with your filters
The list
- Medical device recall ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Reports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Reports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384 Reports of discoloration (residue) on the pins of the skin tensioner have been received by several customers. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trinica Anterior Lumbar Plate (ALP) system, part 07.01058.001 Zimmer Spine, Inc. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ready to Use Thymo-Cide, Germicidal Detergent, containing 0.051% thymol Expired active ingredient was used in the manufacture of the product. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 10 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Georgia, Indiana, Massachusetts, Missouri, Ohio, Oklahoma, South Carolina and Texas named
- Medical device recall BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System Polaris Translation Screw Failures were recently reported to Biomet Spine. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Salter Labs EtCO2 Sample line 15’ It has been determined that three lots of model number 4515-15-25 CO2 Sample Line 15’ tube, male Luer lock connectors may contain a 30’ tube instead of the 15’… Class IIFDA’s classNov 27, 2013in FDA’s Enforcement Report9 statesnamed in where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereFlorida, Michigan, Missouri, Mississippi, North Carolina, New York, Texas, Virginia and Wisconsin
- Medical device recall Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US) The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Georgia, Illinois, Nevada, Ohio, Oklahoma, Tennessee, Texas and Wyoming named
- Medical device recall Fixed Offset Adapter, A-642100 Ossur inititated a voluntary recall of the A-642100 Fixed Offset Adapter because it can develop fatigue cracks in normal use over an extended period of time… Class IIFDA’s classNov 27, 2013in FDA’s Enforcement Report10 statesnamed in where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereAlabama, California, Georgia, Idaho, North Carolina, New Jersey, New York, Texas, Virginia and Wisconsin
- Medical device recall Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical… It was reported that the siderail may appear latched when it is not, due to lack of proper preventive maintenance. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Juggerknotless Drill Bit Investigation identified that the design of the drill bit may make the suture anchor difficult to insert into the bone. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 3 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Indiana and Virginia named
- Medical device recall Siemens Chemistry Calibrator (CAL) used with the ADVIA Chemistry Direct Bilirubin_2 Reagent, Siemens Material… Siemens Healthcare Diagnostics is conducting a field correction for Siemens Chemistry Calibrator Lots 090445B and 090445C on the ADVIA 1200, 1650, 1800, and… Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to visualize upper airway and aid in placement… Labeling inconsistency Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 32 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arizona, California, Colorado, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615 GE Healthcare has recently become aware of a potential safety issue related to a SPECT scan procedure used for pulmonary imaging. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 41 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Wisconsin and West Virginia named
- Medical device recall EPIQ 7 Ultrasound System A problem has been detected with Philips Model EPIQ 7 Ultrasound System, software version 1.0 and 1.0.1. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide, and Connecticut, Hawaii, Illinois, Indiana, Kentucky, Massachusetts, Maine, Michigan, North Carolina, Oregon, Pennsylvania, Texas and Washington named
- Medical device recall Synthes Titanium Trochanteric Fixation Nail (TFN)-Helical Blade Synthes Titanium Trochanteric Fixation Nail… A potential exists for non conforming Synthes Titanium Trochanteric Fixation Nail (TFN)-Helical Blades to be distributed. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Medcare Products Max-500 Stand, Total Support, patient stand The lift might fail with the labeled 500-lb. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Medcare Products Max-500 Stand-N-Weigh, Total Support, patient stand The lift might fail with the labeled 500-lb. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall *** 1) SYMBIQ One-Channel Infuser Hospira shipped the incorrect replaceable battery pack (Part No: HSP3566-E10) instead of the correct E09 battery pack (Part No. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement Report7 statesnamed in where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereKentucky, Minnesota, North Dakota, New Jersey, New York, Pennsylvania and South Dakota
- Medical device recall GE Vivid E9 ultrasound system GE became aware of a potential safety issue due to a system slow down and system lock up associated with the software of Vivid E9 ultrasound system. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Stryker 1) XIA Torque Wrench 2) XIA 3 Torque Wrench 3) XIA Elegance Short Torque Wrench Multiple complaints have reported that the hex tip of the torque wrench fracturing during final tightening. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ExciTE F DSC Soft touch Single Dose, Dual-curing Regular Ref. 50 dental adhesive for restorations Ivoclar Vivadent, Inc. Class IIFDA’s classNov 27, 2013in FDA’s Enforcement Report14 statesnamed in where it went PublishedNov 27, 2013ClassClass IIStatusTerminatedWhereArizona, California, Iowa, Illinois, Indiana, Louisiana, New Jersey, New York, Oregon, Pennsylvania, South Carolina, Texas, Washington and Wisconsin
- Medical device recall Artis zee systems x-ray, angiographic system The firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement Report14 statesnamed in where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereArkansas, Arizona, California, Connecticut, Florida, Iowa, Kansas, Kentucky, Missouri, Montana, New York, Oklahoma, Pennsylvania and West Virginia
- Medical device recall Prostiva RF Therapy Hand Piece Kit A Hand Piece high deployment force exceeded the maximum specification. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 17 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Florida, Georgia, Illinois, Kentucky, Massachusetts, Minnesota, North Carolina, New Jersey, Nevada, New York, Ohio, Oregon, Tennessee, Texas and Utah named
- Medical device recall Applied Medical’s Inzii¿ 12/15mm Retrieval System Applied Medical is conducting a voluntary recall of the Inzii¿ 12/15mm retrieval system. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis use Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator’s manual may disconnect and lead to blood loss Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Combiset Blood Line with BVM for Hemodialysis use Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator’s manual may disconnect and lead to blood loss Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Combiset Blood Line Hemodialysis use Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator’s manual may disconnect and lead to blood loss Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Safire Duo Ablation Catheter MediGuide Enabled St. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 5 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Kentucky, Massachusetts, North Carolina, Ohio and Texas named
- Medical device recall Spacelabs Healthcare elance Vital Signs Monitor Spacelabs Healthcare elance Vital Signs Monitor with Option S, model 93330, is recalled because the monitor will not permit connection of any of the Spacelabs… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedNov 20, 2013ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B)… Baxter Healthcare Corporation is recalling the LCD display screen on the SIGMA SPECTRUM Infusion Pump with Master Drug Library for not meeting standards for… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 30 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Hawaii, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, New Hampshire, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Utah, Virginia, Washington and West Virginia named
- Medical device recall Sterrad 100NX Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX Sterilizer some healthcare workers detected odors/smells emanating from the 100NX… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall DePuy Mitek FMS Intermediary Tubing with One-Way valve Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo intermediary tubing set may not perform as intended. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall DePuy Mitek FMS Outflow Tubing with One-Way valve Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo intermediary tubing set may not perform as intended. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Sarns” Soft-Flow¿ Aortic Cannula without Suture Flange, angled tip, wire-reinforced with luer port, aortic… During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement Report9 statesnamed in where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereCalifornia, District of Columbia, Louisiana, Massachusetts, Michigan, Missouri, Oklahoma, Texas and Wisconsin
- Medical device recall Sarns” Soft-Flow¿ Aortic Cannula without Suture Flange, straight tip, wire-reinforced with luer port, aortic… During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement Report9 statesnamed in where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereCalifornia, District of Columbia, Louisiana, Massachusetts, Michigan, Missouri, Oklahoma, Texas and Wisconsin
- Medical device recall Sarns” Soft-Flow¿ Aortic Cannula without Suture Flange, straight tip, wire-reinforced with luer port, aortic… During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement Report9 statesnamed in where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereCalifornia, District of Columbia, Louisiana, Massachusetts, Michigan, Missouri, Oklahoma, Texas and Wisconsin
- Medical device recall Sarns” Venous Return Cannulae, 20 Fr with 1/4” flare, 14.5” During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS) identified the presence of loose fiber particulate that exceeded finished product… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement Report9 statesnamed in where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereCalifornia, District of Columbia, Louisiana, Massachusetts, Michigan, Missouri, Oklahoma, Texas and Wisconsin
- Medical device recall SIGMA SPECTRUM Infusion Pump with Master Drug Library Baxter Healthcare Corporation issued an Urgent Device Correction for the SIGMA SPECTRUM Infusion Pump with Master Drug Drug Library due to reports of upstream… Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportPuerto Ricothe one state its words name PublishedNov 20, 2013ClassClass IIStatusTerminatedWherePuerto Rico
- Medical device recall Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the Pneumatic Motor Systems… Anspach Effort, Inc. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems including:… Anspach Effort, Inc. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Product Catalog (part number 20-0020) utilized with the Electric and Pneumatic Motor Systems including:… Anspach Effort, Inc. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Titan 3T MRI System, MRT-3010A/5 Toshiba America Medical Systems, Inc. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 12 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Georgia, Iowa, Indiana, Louisiana, Nevada, New York, Oregon, Pennsylvania, Texas and Wisconsin named
- Medical device recall Synthes 8.5 MM Medullary Reamer Product Usage: An orthopedic manual surgical instrument is a nonpowered… Complaints were received for intraoperative reamer head breakages which can allow for unretrieved fragments of non-implant grade material. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Plum A+ Hyperbaric Infusion Pump Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, 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, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Plum A+ Infusion Pump Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, 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, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Plum A+ Infusion Pump Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, 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, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
- Medical device recall Plum A+3 Infusion Pump System Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. Class IIFDA’s classNov 20, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 51 states named PublishedNov 20, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, 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, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, US Virgin Islands, Vermont, Washington, Wisconsin, West Virginia and Wyoming named
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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