PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: September 25, 2024 Initiated: July 18, 2024 #Z-3150-2024

Product Description

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.

Reason for Recall

There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.

Details

Units Affected
4 units
Distribution
US, Colombia, Philippines, Russia
Location
Maple Grove, MN

Frequently Asked Questions

What product was recalled?
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.. Recalled by Boston Scientific Corporation. Units affected: 4 units.
Why was this product recalled?
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 25, 2024. Severity: Moderate. Recall number: Z-3150-2024.