HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545940
FDA Recall Z-0325-2022 · Posted None
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Recalling FirmBoston Scientific Corporation
Recall StatusOpen, Classified
Product CodeFGE
Date Initiated2021-10-21
Reason for Recall
Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
Firm Action
Boston Scientific issued Urgent Medical Device Removal Letter to US consignees via Federal Express Priority Overnight mail on October 21, 2021. Letter states reason for recall, health risk and action to take:
Cease further distribution or use of any remaining product affected by this
removal immediately.
Verify by product lot/batch number in the product table whether any product within your
inventory is affected. If so, indicate on your Reply Verification Tracking Form the
quantity of units from each lot/batch that you will be returning.
If you identify any product from the affected lots/batches within your inventory, please
segregate the product immediately and return it to BSC in accordance with the enclosed
instructions. If you are a distributor, please note that the depth of this removal is to
the end user level and this notification should be forwarded to your customers. If
you are a facility that has sent products to another hospital or facility within your
network, please ensure that this notification is forwarded to them.
Please read carefully through the removal instructions included with this notification.
Your local Sales Representative can answer any questions that you may have
regarding this notification.
Root Cause
Device Design
Distribution Pattern
US Nationwide distribution.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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