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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Arrow International Inc: Potential leak in the balloon extension line. If a leak was present and went undetected during pre-use testing as outlined in the IFU, this would cause the balloon to deflate slowly following placement. If the leak went undetected by attending clinicians during use, it could result in contrast injection into the vascular or cardiac tissue which could result in serious injury or death

Agency Publication Date: December 19, 2019
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Affected Products

Product: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130

Lot Number: 16F19H0089

Lot Numbers:
Number
Product: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J

Lot Number: 16F19H0093

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84399
Status: Resolved
Manufacturer: Arrow International Inc
Manufactured In: United States
Units Affected: 2 products (71 units; 1 unit)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.