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FDAFDA · Food and drugs·Recall number Z-2256-2017

Arrow Pressure Injectable PICC Kit The Arrow International Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling

Published June 14, 2017 · Recall initiated: March 20, 2017

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Arrow International Inc
Distributor
Nationwide Distribution
Lot
510K # K061289; Material numbers: EU-04041-HPMSB, EU-04052-HPMSB, EU-05041-HPMSB, and EU-05052-HPMSB.
Risk classification
Class II
Area (FDA)
device
Country
United States

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