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 6, 2026.
2,249of 2,249 medical device recallsshown with your filters
The list
- Medical device recall Sybron Endo Lightspeed: LSX Files, 25MM The length markings on the Lightspeed LSX files were wrong. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNo state named
- Medical device recall P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging and produced smoke with a chemical… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Phillips Easy Diagnost Eleva DRF The mirror icon on the bottom of each image could be misinterpreted as a RIGHT lead marker for side indication if the image is mirrored within a PACS system. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 8 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Delaware, Florida, Kentucky, Missouri, North Carolina and Washington named
- Medical device recall Li-Ion battery used in the Oxus Portable Oxygen Concentrator (POC), RS-00400 Due to past battery inventory storage conditions and deficiencies in the maintenance procedure, it was possible that some batteries were over-discharged to… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement Report16 statesnamed in where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereAlabama, California, Colorado, Florida, Georgia, Iowa, Illinois, Michigan, New York, Ohio, Oklahoma, Oregon, Texas, Utah, Wisconsin and West Virginia
- Medical device recall Trilogy F/M Acetabular Shell without holes Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy F/M Acetabular Shell without holes SOLID HA Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy F/M Acetabular Shell with Uni-Hole Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy Acetabular Shell Spiked Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy Acetabular Shell with Cluster Holes Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy Acetabular AB Shells with Cluster Holes Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy Acetabular Shells with Holes Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Trilogy Acetabular AB Shells with Holes Some units of Trilogy shells manufactured since March 2009 may be below the lower range of the pore size specification (as low as 28% vs. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall PREMIER LIFECARE RECLINER 5400 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 A multi… The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Illinois, Massachusetts, Maryland, Minnesota, New Mexico, New York, Ohio, Oklahoma and Texas named
- Medical device recall PREMIER CARE RECLINER 5570/5574 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Illinois, Massachusetts, Maryland, Minnesota, New Mexico, New York, Ohio, Oklahoma and Texas named
- Medical device recall Cozy Comfort Premier Recliner 5580 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Illinois, Massachusetts, Maryland, Minnesota, New Mexico, New York, Ohio, Oklahoma and Texas named
- Medical device recall Designer Care Cliner 6700/6704/6710 WITH CAL TB 133 UPGRADE PURCHASED JAN 01, 2011 TO AUGUST 20, 2012 The performance of the chemicals in the foam and vinyl are not consistent enough to meet the TB 133 fire protection mandate required by California and 4 other… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Florida, Illinois, Massachusetts, Maryland, Minnesota, New Mexico, New York, Ohio, Oklahoma and Texas named
- Medical device recall Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill… Although the reported incidence is low, there is the potential for the drill stop to slip on the drill bit resulting in an adverse event. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, 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, West Virginia and Wyoming named
- Medical device recall Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion, Adjustable… Although the reported incidence is low, there is the potential for the drill stop to slip on the drill bit resulting in an adverse event. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 52 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alaska, 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, West Virginia and Wyoming named
- Medical device recall Anspach Effort, Inc., 98-0061 MA-15C Bearing Sleeve with Removable Bur Guard Contact between the bur and bur guard could generate metal fragments that may or may not be visible to the surgeon and can potentially remain in the surgical… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportMassachusettsthe one state its words name PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereMassachusetts
- Medical device recall THERA PEARL 3-in-1 BREAST THERAPY, 2 hot and cold packs in plastic box The Spanish translation on the Instructions for Use (IFU) insert and product package for hot and cold packs has incorrect heating instructions which would… Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California, Illinois, Minnesota, North Carolina, New Jersey, New York, Pennsylvania, Rhode Island, South Dakota, Texas and West Virginia named
- Medical device recall Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to a sitting… The potential exists for the wheel to rotate freely despite engagement of hub brake. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 2 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and California and Montana named
- Medical device recall Exactech NOVATION CROWN CUP, NEUTRAL LINER, Use with Crown Cup Only, GXL UHMWPE, SN 0123456 Recall of Novation Crown Cup Connection GXL Neutral Liners Catalog No. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement Report5 statesnamed in where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereFlorida, Nevada, Tennessee, Virginia and Washington
- Medical device recall Exactech NOVATION CROWN CUP +5mm LATERALIZED LINER, Use with Crown Cup Only, GXL UHMWPE, SN 0123456 Recall of Novation Crown Cup Connection GXL Neutral Liners Catalog No. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement Report5 statesnamed in where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereFlorida, Nevada, Tennessee, Virginia and Washington
- Medical device recall ConMed Linvatec Biomaterials, PopLok bone Punch PKL-35M, 3.5mm Orthopedic manual surgical instrument - Bone… ConMed Linvatech recalled one lot of their PopLok bone Punch 3.5mm because the metal shaft diameter is 4.5mm when it should be 3.5mm. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportCaliforniathe one state its words name PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereCalifornia
- Medical device recall Oxoid Antimicrobial Susceptibility Test Discs, Aztreonam 30 ug, IVD The firm is recalling the product due to some cartridges may contain individual discs that are not impregnated with antibiotic. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 13 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Connecticut, Illinois, Massachusetts, Maryland, Missouri, North Carolina, New Jersey, Rhode Island, Texas, Washington and Wisconsin named
- Medical device recall Medacta Quadra Trial Broach size 0 part # 01.10.10.045, for use with the Medacta Total Hip Prosthesis System The tip of the Quadra Trial Broach size 0, broke during a surgery. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 9 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arizona, California, Idaho, Illinois, North Carolina, Ohio, Utah, US Virgin Islands and Washington named
- Medical device recall Diagnostic Hybrids, Inc., RhMK RhMK product fungal contamination. Class IIIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 38 states named PublishedFeb 13, 2013ClassClass IIIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington and Wisconsin named
- Medical device recall OPTIGEN Food 30 There is no evidence that a visual inspection was performed on one tray of coverslips. Class IIIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNot namedno state, in where it went PublishedFeb 13, 2013ClassClass IIIStatusTerminatedWhereNo state named
- Medical device recall SeriScaffold Surgical Scaffold Product Number: SCF10X25AGEN Product is dual packaged in an inner and outer pouch, the outer pouch seal may be compromised and sterility may not be assured Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement Report13 statesnamed in where it went PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereCalifornia, Florida, Georgia, Michigan, Minnesota, New Jersey, New York, Ohio, Oregon, Rhode Island, Texas, Virginia and Washington
- Medical device recall Custom Breast Biopsy Tray Surgical procedure trays are packed with pharmaceuticals for injection that may contain particulate matter. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Georgia, Maine, North Carolina and Ohio named
- Medical device recall Custom Breast Biopsy Tray w/Sodium Chloride Surgical procedure trays are packed with pharmaceuticals for injection that may contain particulate matter. Class IIFDA’s classFeb 13, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 13, 2013ClassClass IIStatusTerminatedWhereNationwide, and Georgia, Maine, North Carolina and Ohio named
- Medical device recall Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products It was discovered the CS3000/CS3070 was manufactured using the laser power settings for a Class 2 laser device instead of the Class 1 power levels as specified… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose Values of fluoroscopy time, Air Kerma Rate and Cumulated Air Kerma may not be displayed “at the fluoroscopist’s working position” as per 21 CFR 1003.21 Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 11 states named PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, California, Colorado, Connecticut, Illinois, Maryland, Michigan, Missouri, New York, Ohio and Pennsylvania named
- Medical device recall BacT/ALERT SA Blood Culture Bottle BacT/ALERT SA Culture Bottle lot 1031866 may contain bottles with uncured sensors. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report29 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereArkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Michigan, Minnesota, Missouri, North Carolina, New Jersey, New York, Ohio, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Wisconsin and West Virginia
- Medical device recall BBL(TM) Fildes Enrichment Enrichment media intended to enhance the cultivation of various microorganisms may fail to support the growth of Haemophilus species. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device Affected lots of Cordis ExoSeal (TM) VCD have been sterilized using a process that did not achieve the sterility assurance level that is required by the… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 44 states named PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide, and Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Hawaii, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin and West Virginia named
- Medical device recall HAMILTON-T1 Ventilator with software versions 1.1.2 or lower Analysis of a customer complaint has shown that during ventilation of small pediatric patients with high airway resistance and low lung compliance, the oxygen… FDA Class I, its most serious class Class IFDA’s class (needs attention)Feb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IStatusTerminatedWhereNationwide
- Medical device recall Mindray DPM5 Monitor, a vital signs monitor used on human patients in healthcare facilities. Mindray has identified an issue with the DPM5 monitors where ST and Arrhythmia features may not be available. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 4 states named PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide, and Florida, Tennessee, Texas and Virginia named
- Medical device recall Alfa Wassermann System Diluent 750 mL Inorganic phosphorus assays using System Diluent Lot 155599 may not product acceptable calibration results. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Dimension(R) IRON Calibrator (DC85), Siemens material number 10445010 Siemens Healthcare Diagnostics has received complaints of IRON calibrations outside of acceptable calibration slope (m) values (0.97 - 1.03) when using IRON… Class IIIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIIStatusTerminatedWhereNationwide
- Medical device recall Alere Cholestech LDX Multianalyte Control, 2 vial set Out of range (increased) HDL Cholesterol results. Class IIIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedFeb 6, 2013ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Alere Cholestech LDX Calibration Verification, 4 vial set Out of range (increased) HDL Cholesterol results. Class IIIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 1 state named PublishedFeb 6, 2013ClassClass IIIStatusTerminatedWhereNationwide, and Puerto Rico named
- Medical device recall Esteem Programmer Envoy Medical is conducting a voluntary correction of a limited number of Esteem Programmers, part of the Esteem Totally Implantable Hearing System, to reduce… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report14 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereAlabama, Arizona, California, Connecticut, Florida, Georgia, Illinois, Massachusetts, Michigan, Minnesota, North Carolina, Oklahoma, Rhode Island and Texas
- Medical device recall 45¿ Angle Driver / Z-H, Greatbatch Medical 10 000 Wahrie Drive, Clarance, NY 14031 Greatbatch Medical has initiated a global voluntary recall and market withdrawal of its entire Small Angled Driver 45¿ product line. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report8 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereCalifornia, Indiana, Kansas, Massachusetts, New Jersey, Pennsylvania, Tennessee and Texas
- Medical device recall Extremity Medical, IO FiX System Accessory Lag screw measurement is short (approximately 5 mm) when using current screw measuring device (p/n 101-00010) per the IO FIX Surgical Technique Rev C. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word, and 20 states named PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide, and Arkansas, Arizona, California, Florida, Georgia, Illinois, Indiana, Maryland, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Tennessee, Texas, Washington and Wisconsin named
- Medical device recall TUNNELOC ROUND HEAD INTERFERENCE SCREW 8MMX25MM Biomet Sports Medicine manufactures a variety of internal… Thru hole at the tip of the screw is undersized. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report7 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereAlabama, California, Florida, Illinois, Kentucky, Ohio and Texas
- Medical device recall AdvantageSim MD versions 7.4 through 7.6 It was reported by a customer site that when using GE AdvantageSim MD on Advantage Workstation, the series could be incorrectly labeled in image view when… Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement Report13 statesnamed in where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereAlabama, Connecticut, Florida, Illinois, Massachusetts, Missouri, New Jersey, New York, Pennsylvania, Texas, Virginia, Washington and Wisconsin
- Medical device recall Ortho Clinical Diagnostics VITROS¿ Chemistry Products Vapor Adsorption Cartridge REF/CAT No. 680 0100 Some VITROS¿ Chemistry Products Vapor Adsorption Cartridge CAT No. Class IIFDA’s classFeb 6, 2013in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedFeb 6, 2013ClassClass IIStatusTerminatedWhereNationwide
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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