FDA Announces Class I Recall On Arrow International Cardiac Catheter Device

The US FDA has announced a high-risk class I recall  on a cardiac catheter from Teleflex Inc. subsidiary Arrow International due to the risk of tip damage during use.

Recall Road Sign against sky.
• Source: Shutterstock

A cardiac catheter from Teleflex Incorporated subsidiary Arrow International Inc. is the subject of a high-risk class I recall due to the risk of tip damage during use, the US Food and Drug Administration announced on 23 February.

The Arrow-Trerotola Percutaneous Thrombolytic Device, or PTD, consists of a catheter with an expandable basket attached to a drive cable....

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