Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Reported: June 14, 2017 Initiated: March 20, 2017 #Z-2297-2017
Product Description
Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
Reason for Recall
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Details
- Recalling Firm
- Arrow International Inc
- Units Affected
- unknown-firm reports total devices distributed 43,394
- Distribution
- Nationwide Distribution
- Location
- Reading, PA
Frequently Asked Questions
What product was recalled? ▼
Radial Artery Catheterization Kit with Sharps Safety Features The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels. Recalled by Arrow International Inc. Units affected: unknown-firm reports total devices distributed 43,394.
Why was this product recalled? ▼
Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 14, 2017. Severity: Moderate. Recall number: Z-2297-2017.
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