FDA Medical Device Recalls (openFDA)
Boston Scientific Corporation: vanSonnenberg Sump Locking Pigtail Regular Kit Sump Catheter System Kit, Material Number REF M001273090; for use as a percutaneously placed drain for intra-abdominal fluid collections.
- Recall number
- Z-3150-2024
- Recalling firm
- Boston Scientific Corporation
- Product
- vanSonnenberg Sump Locking Pigtail Regular Kit Sump Catheter System Kit, Material Number REF M001273090; for use as a percutaneously placed drain for intra-abdominal fluid collections.
- Status
- Open, Classified
- Initiated
- 2024-07-18
- Posted
- 2024-09-13
- Terminated
- not on file
- Reason
- There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
- Root cause
- Packaging process control
- Action
- Boston Scientific issued am Urgent Medical Device Removal notice to it consignees on 07/18/2024 via overnight mail. The notice explained the issue, potential hazard, and requested the return of the devices. Consignees were directed to post the notice in a visible location near the affected products to ensure visibility and to share the notice with all those to whom the device was transferred. Distributors were direct to notify their customers.
- Quantity
- 4 units
- Distribution
- US, Colombia, Philippines, Russia
- Lot, serial or model codes
- GTIN/UDI 0871472913774, Lot # 33512377, exp. 02/26/2027
- 510(k) numbers
- ["K211934"]
- PMA numbers
- not on file
- Product code
- FFA
- Firm FEI
- 3002095335
- Firm city
- Maple Grove
- Firm state
- MN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28