Arrow Central Venous Catheter Kits Recalled for Needlestick Injury Risk
Arrow International is recalling certain central venous catheter 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 reported needlestick injuries, which constitute significant injury reports, meeting the criteria for a Severe (Score 4) classification.
Plain-English summary
Arrow International Inc. has initiated a recall of Pressure Injectable Multi-Lumen Central Venous Catheterization Kits with Blue FlexTip, ARROWg+ard Blue PLUS Catheter, and Sharps Safety Features. The recall is due to reports of safety cover disengagement and needlestick injury associated with the BD Eclipse Needle packaged with these products.
The affected product is identified by material number ASK-42703-PRJ. The recall involves nationwide distribution. The ARROWg+ard Blue Plus antimicrobial catheter is indicated for short-term central venous access in various medical treatments.
Healthcare facilities and consumers should stop using the affected kits and contact Arrow International for further instructions or replacement.
The recalled product
- Product
- Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features The ARROWg+ard Blue Plus" antimicrobial catheter is indicated in the short-term ( < 30 days) treatment of diseases or conditions r
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Catheters
- Hazard
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-42703-PRJ
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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