Recalls / —
—#177416
Product
Boston Scientific Advanix Pancreatic Stent, Straight Leading Barb, 10F x 10cm UPN: M005336680
- FDA product code
- FGE — Stents, 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: 21285272 21568464 21750673 21865109 22072355 22613957 23408730 23492662
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 #177416. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.