Arrow International Recalls Central Venous Catheter Kits Due to Needlestick Risk
Arrow International is recalling 43,394 central venous catheter kits because the packaged BD Eclipse Needle may disengage, posing a needlestick injury risk.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (needlestick injury) where injury has been reported, but the source does not specify FDA Class I or fatalities, fitting the High severity criteria.
Plain-English summary
Arrow International Inc. is recalling 43,394 units of the Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter. The recall is due to reports of safety cover disengagement and needlestick injury associated with the BD Eclipse Needle packaged with these specific Arrow products.
The affected product is identified by Material # ASK-15703-PST. The Arrow CVC is indicated for short-term central venous access for various medical treatments. The recall covers nationwide distribution.
Healthcare facilities and consumers should stop using the affected kits and contact Arrow International for further instructions on handling or replacement.
The recalled product
- Product
- Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter The Arrow(r) CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limite
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Catheters
- 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 # ASK-15703-PST
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.
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