The Recall Desk
SevereFDA (Devices)·Z-2297-2017·Announced 2017-06-14

Arrow Radial Artery Catheterization Kit Recalled for Needlestick Injury Risk

Arrow International is recalling Radial Artery Catheterization Kits because the packaged BD Eclipse Needle safety cover may disengage, posing a needlestick injury risk.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall involves a medical device with reported needlestick injuries, which constitutes a significant injury report under the severity rubric.

Plain-English summary

Arrow International Inc. is recalling the Radial Artery Catheterization Kit with Sharps Safety Features. The recall is initiated due to reports of safety cover disengagement and needlestick injury associated with the BD Eclipse Needle packaged with certain Arrow products.

The affected product is identified by material number ASK-04020-MUSC. The firm reports that a total of 43,394 devices were distributed nationwide. The Arrow Arterial Catheterization device is designed to permit access to the peripheral arterial circulation or to other small vessels.

Healthcare facilities and consumers should stop using the affected kits and contact Arrow International Inc. for further instructions or a replacement.

The recalled product

Product
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
Affected units
43,394

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Material number ASK-04020-MUSC

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 56 recalled by Arrow International Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 56 products in this recall →