Arrow International Recalls Central Venous Catheter Kits with Incorrect Guide
Arrow International is recalling 5,926 central venous catheterization kits distributed nationwide because they may contain the incorrect Springwire Guide.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a temporary or medically reversible adverse health consequence. The source text does not report any specific injuries or illnesses, indicating a precautionary recall for a component error.
Plain-English summary
Arrow International Inc is recalling 5,926 units of the Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features. The affected product code is ASK-15703-PRWJ, with expiration dates ranging from February 2018 to November 2018. The specific lot number is 13F17C0400.
The recall was initiated because these finished good kits may contain the incorrect Springwire Guide (SWG). The products were distributed nationwide in the United States.
Healthcare facilities and consumers should stop using the affected kits and contact Arrow International Inc for further instructions or a return.
The recalled product
- Product
- Pressure Injectable Multi Lumen Central Venous Catheterization Kit with Blue FlexTip Catheter and Sharps Safety Features; Product Code: ASK-15703-PRWJ; Exp. Dates Feb 2018- Nov 2018
- Manufacturer
- Arrow International Inc
- Category
- Medical Device — Catheters
- Hazard
- Affected units
- 5,926
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)
- Lot number: 13F17C0400
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 12 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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