FDA Device Recalls

Recalls /

#177415

Product

Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 9cm UPN: M00536670

FDA product code
FGEStents, Drains And Dilators For The Biliary Ducts
Device class
Class 2
Medical specialty
Gastroenterology, Urology
510(k) numbers
K133700
Affected lot / code info
Lot Numbers: 21376782  21636753  21724127  21833853  22007181  22136472  22195529  22212529  22522255  22613956  22858807  23073638  23321211  23408729  23875252  24167479  24229866  24411528

Why it was recalled

Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life

Root cause (FDA determination)

Incorrect or no expiration date

Action the firm took

Boston Scientific issued Notifications to consignees via Federal Express Priority mail on October 21, 2019. The notification instructs the account to check their inventory remove any affected product from their inventory, and return it to Boston Scientific. The notification also requests the completion of a Reply Verification Tracking Form.

Recalling firm

Firm
Boston Scientific Corporation
Address
300 Boston Scientific Way, Marlborough, Massachusetts 01752-1291

Distribution

Distribution pattern
Nationwide Foreign: Austria Australia Belgium Bulgaria Croatia Czech Rep Denmark Finland France Germany Great Britain Italy Japan Pakistan Poland Russian Fed. Slovakia South Africa Spain Sweden Switzerland Thailand Turkey

Timeline

Recall initiated
2019-10-21
Posted by FDA
2019-11-25
Terminated
2023-12-20
Status

Source: openFDA Device Recall endpoint. Recall record ID #177415. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

— recall: Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 9cm UPN: M00536670 · FDA Device Recalls