FDA recall record

Boston Scientific HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of recall — FDA Z-0326-2022

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

Class IIclassification
Z-0326-2022official record ID
Dec 8, 2021report date

Recall record at a glance

Official recordZ-0326-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBoston Scientific Corporation
Report dateDec 8, 2021
Recall initiation dateOct 21, 2021
LocationMarlborough, MA, United States

Official product description

HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950

Why the product was recalled

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

Distribution information

US Nationwide distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: not stated.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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