Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm (OUS) UPN: M00553550 - Product Usage: The stent is intended for implantation up to 60 days and should be removed upon confirmation of pseudocyst or walled-off necrosis resolution.
FDA Recall Z-0777-2021 · Posted None
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Recalling FirmBoston Scientific Corporation
Recall StatusTerminated
Product CodePCU
Date Initiated2020-12-01
Date Terminated2023-07-14
Product Quantity61 units
Reason for Recall
The rotating luer fitting at the distal end of the
delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or use, resulting in delay or procedure or
risk of peritonitis developing from leakage of enteric, pseudocyst, or biliary contents into the peritoneal cavity
Firm Action
Boston Scientific issued customer notification letters to consignees via Federal Express Priority Overnight mail on December 1, 2020. The 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.
Your local Sales Representative can answer any questions that you
may have regarding this notification.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution - Foreign: TBD.
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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