Medical Device Recalls

This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.

Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.

38,428 total recalls
0 this month

Showing 24601–24620 of 38,428 recalls

March 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue Large-Bore Multi-Lumen CVC Kit. The large-bore...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue (R)

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology A PICC permits venous access

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) Access Kit for use with 4 Fr. Peripherally Inserted

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ VPS¿ Access Kit with Maximal Barrier Precautions for use

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit The Arrow¿ Arterial Catheterization device...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: "Pressure Injectable Jugular Axillo-Subclavian Central Catheter (JACC)...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
March 20, 2017· Arrow International Inc

Recalled Item: Arterial Catheterization Kit with Maximal Barrier Precautions The Arrow¿...

The Issue: Arrow International initiated the recall due to reports

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated