Vertical Drain Tube Device (Hollister) – Tube Holder Separation (2021)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
Brand
Hollister Incorporated
Lot Codes / Batch Numbers
Model: 9782. UDI: Primary Unit of Use DI Number: 00610075097821. Lot Numbers: 0K02, 1A09, and lAlO
Products Sold
Model: 9782. UDI: Primary Unit of Use DI Number: 00610075097821. Lot Numbers: 0K02, 1A09, and lAlO
Hollister Incorporated is recalling Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage due to The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder has the potential failure to separate fr. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder has the potential failure to separate from the barrier. This separation might contribute to the potential risk of the tube/drain/catheter migration or loss.
Recommended Action
Per FDA guidance
Hollister has instructed the affected consignees to quarantine the affected inventory and discard the product per their local procedures for product destruction.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026