Medical devices, 2018
Shortlist up to four to read them side by side.
3,757 medical device recalls FDA’s Enforcement Report published in 2018, 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.
3,757of 3,757 medical device recallsshown with your filters
The list
- Medical device recall Bronchovideoscope BF-MP60 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-P160 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-P180 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-P240 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchofiberscope BF-P40 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchofiberscope BF-P60 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-Q180 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-Q180-AC The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultrasonic Bronchoscope BF-UC160F-OL8 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Ultrasonic Bronchoscope BF-UC180F The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-XP160F The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchofiberscope BF-XP40 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchofiberscope BF-XP60 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-XT160 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchofiberscope BF-XT40 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Rhino Laryngo scope ENF-VT2 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Airway Mobilescope MAF-TM The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Bronchovideoscope BF-1T40 The attachment of non-Olympus accessories to the bronchoscope s instrument channel port may have resulted in more applied force than expected and lead to… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTI TUOHY ULTRA 360 2 IN CONT PNB SET, Material Number 331640 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNBFX350O CONTIPLEX CONT NERVE BLOCK, Material Number 331670 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNBFX350C CONTIPLEX CONT NERVE BLOCK, Material Number 331672 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX TUOHY ULTRA 2 IN CONT The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNB200T CONTIPLEX TUOHY SET 2 IN, Material Number 331691 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX TUOHY ULTRA 4 IN CNB400TU, LF, Material Number 331691 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX TUOHY SET, 18GX4”, 1.3X100MM, Material Number 331693 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX TUOHY SET, 18GX6”, 1.3X150MM, Material Number 331694 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX TUOHY SET, 18GX11/2X 1,3X40MM, Material Number 331695 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNB200S CONTIPLEX INSULATED TUOHY NDL, Material Number 331697 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNB200TK CONTIPLEX CONT NERVE BLOCK, Material Number 331701 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CNB400TK CONTIPLEX CONT NERVE BLOCK, Material Number 331706 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall SCNB4TK CONT STIM W/4 INCH INSUL TUOHY, Material Number 331756 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONT STIM BASIC KIT W/2 IN INSUL TUOHY, Material Number 331757 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONT STIM BASIC KIT W/4 IN INSUL TUOHY, Material Number 331758 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTIPLEX ECHO OT W/4” TUOHY ULTRA SET, Material Number 331762 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CONTI ECHO CT W/2IN TUOHY ULTRA 360 SET, Material Number 331767 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFCY 17GA SAFETY TUOHY NEEDLE TRAY, Material Number 332075 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY, Material Number 332077 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFCPS EPIDURAL FULL TRAY, Material Number 332078 Connection device used by physicians to provide various… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFC EPIDURAL TRAY W/ 17GA TUOHY, Material Number 332079 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFSA FULL TRAY W/17G TUOHY 19G SPRW, Material Number 332080 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE18TKST CONT EPID W/SOFT TIP, Material Number 332081 Connection device used by physicians to provide various… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKST CONT EPID W/SOFT TIP, Material Number 332082 Connection device used by physicians to provide various… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE18HKST CONT EPID 20G SOFTIP, Material Number 332084 Connection device used by physicians to provide various… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKF PERIFIX CONTIN The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFPS PERIFIX FX CONT The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFSDT EPID TRAY W/17GA FIXED WING, Material Number 332093 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFSDTD EPID TRAY W/17GA FIXED WING, Material Number 332095 Connection device used by physicians to… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall CE17TKFMHDT 17 GA X 4 FULL EPID KIT, Material Number 332096 Connection device used by physicians to provide… The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been… Class IIFDA’s classOct 10, 2018in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedOct 10, 2018ClassClass 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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