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 6, 2026.
2,615of 2,615 medical device recallsshown with your filters
The list
- Medical device recall ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit The MAC(TM) Multi-Lumen Central Venous Access Device… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow VPS Access Kit with Maximal Barrier Precautions for use with 5 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter The Arrow(r)… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R) Access Device, Integral Hemostasis… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostatis Valve/Side Port,… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure injectable… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARROWg+ard Blue MAC Two-Lumen Central Venous Access Kit Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit The large-bore multiple-lumen catheter permits venous access… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow PICC with Chlorag+ard Technology A PICC permits venous access to the central circulation through a… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure injectable Jugular Axillo-Subclavian Central CThe CG+Arrow JACC powered by Arrow VPS Stylet permits… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter The… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit The ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AGB+ Pressure Injectable Multi-Lumen CVC Kit intended to permit venous access to the central circulation by… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall AGB+ Pressure Injectable Multi-Lumen CVC Kit The Arrow Central Venous Catheters are intended to permit venous… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow(R) VPS(R) Access Kit for use with 4 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow(R) VPS(R) Access Kit for use with 5 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The ArrowEVOLUTIONTM Pressure Injectable… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow PICC with Chlorag+ard Technology The ArrowEVOLUTION Pressure Injectable PICC with Chlorag+ard… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow¿ Access Kit with Maximal Barrier Precautions for use with 4 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow(R) Access Kit for use with 4 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow¿ Access Kit with Maximal Barrier Precautions for use with 5 Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arrow PICC with Chlorag+ard Technology A PICC permits venous access to the central circulation through a… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall “Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC) Product” The CG+ Arrow JACC powered by… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port for use with 7 - 7.5¿¿Fr Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall QuickFlash Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow¿ Arterial Catheterization device… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass IIStatusTerminatedWhereNationwide
- Medical device recall Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions The Arrow¿ Arterial… Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with… Class IIFDA’s classJun 14, 2017in FDA’s Enforcement ReportNationwideFDA’s word for where it went PublishedJun 14, 2017ClassClass 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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