Arrow QuickFlash Radial Artery Catheterization Kit Recalled for Needlestick Risk
Arrow International is recalling QuickFlash Radial Artery Catheterization Kits because the packaged BD Eclipse Needle 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 Class II medical device with reported needlestick injuries, which constitutes significant injury reports under the severity rubric.
Plain-English summary
Arrow International Inc. is recalling the QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit. The recall is initiated due to reports of safety cover disengagement and needlestick injury associated with the BD Eclipse Needle that is packaged with certain Arrow products.
The affected product is identified by material number ASK-04500-HF-S. 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 users should stop using the affected kits and contact Arrow International Inc. for further instructions regarding the recall and potential replacement or refund.
The recalled product
- Product
- QuickFlash(R) Radial Artery/Arterial Line Catheterization Kit The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels
- Manufacturer
- Arrow International Inc
- Hazard
- 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-04500-HF-S
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 →Related recalls
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