Use caution Medical device recall · FDA · Published February 11, 2021

Hollister VTAD Gastrointestinal Tube Device Recall: Risk of Tube Migration

Hollister recalls VTAD gastrointestinal tube attachment devices (model 9782) due to potential tube separation causing migration or loss. Affected units include specific lot numbers. Consumers should contact Hollister for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1311-2021Medical device Hollister ›

Use caution until it’s fixed

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.

Take action

Contact the company

Recalling firmHollister Incorporated2000 Hollister Dr · Libertyville, IL 60048-3781

✎ GovInfoNow plain-language explainer

Holl: The Hollister VTAD gastrointestinal tube attachment device (model 9782) is recalled because the tube holder can separate from the barrier securing it to the patient's body. This separation might cause the tube to migrate or become lost, posing a risk of injury. Read more at govinfonow.com/recall/63280-hollister-vtad-gastrointestinal-tube-device-recall-risk-of-tube-migration.

Source Summary by GovInfoNow · govinfonow.com/recall/63280-hollister-vtad-gastrointestinal-tube-device-recall-risk-of-tube-migration · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1311-2021

Cite this page

“Hollister VTAD Gastrointestinal Tube Device Recall: Risk of Tube Migration.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63280-hollister-vtad-gastrointestinal-tube-device-recall-risk-of-tube-migration. Based on FDA recall #Z-1311-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1311-2021%22&limit=1).

Hollister Incorporated voluntarily recalled the Vertical Drain Tube Attachment Device (VTAD) on Feb. 11, 2021, according to the FDA. The tube holder can separate from the barrier, potentially causing catheter migration or loss.

How to tell if you have it

Brand: Hollister
Product: Vertical Drain Tube Attachment Device (VTAD)
Model: 9782
UDI: 00610075097821
Lot Numbers: 0K02, 1A09, and lAlO
Quantity: 1,031 boxes (5,155 eaches)
Distribution: US Nationwide including IL, CO, NJ, CA, AZ, TX, KS, NY, IN, SC, RI, ID, WV, OH, MT, MO, SD, MI, MA, PA, VA, FL, NE, OR, KY, GA, WA, OK, TN, NC, MD, MN, MS, LA, NM, ND and Canada

The hazard

The tube holder can separate from the barrier that secures the device to the patients' body. This separation might contribute to the potential risk of the tube/drain/catheter migration or loss.

Context

GovInfoNow's records show Hollister Incorporated has 1 other recall on record since 2024-12-23, including the 2024-12-23 Hollister AnchorFast SlimFit Tube Fastener Recall for skin barrier wear time risk. Other recent recalls of similar products include Elekta Geneva Brachytherapy Applicator Recall (2026-04-03), Elekta Fletcher CT/MR Shielded Applicator Set Recall (2026-04-03) and Elekta Advanced Gynecological Applicator Recall (2026-04-03).

How to tell if you have this one

Check for the model number 9782 on the device. Affected units include lot numbers 0K02, 1A09, and lAlO. The device is used to stabilize and secure gastrointestinal tubes and surgical drains.

Brand
Hollister
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Model
Look for model number 9782 on the device to confirm if it's affected.
Contact Hollister
Reach out to Hollister Incorporated for specific instructions on next steps.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 36 states.

FDA distribution: “Worldwide distribution - US Nationwide distribution including in the states of IL, CO, NJ, CA, AZ, TX, KS, NY, IN, SC, RI, ID, WV, OH, MT, MO, SD, MI, MA, PA, VA, FL, NE, OR, KY, GA, WA, OK, TN, NC, MD, MN, MS, LA , NM, ND and the country…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arizona, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, West Virginia.

Recall timeline

FDA terminated this recall 19 months after the firm started it.

Feb 11, 2021Firm started the recall
Mar 26, 2021FDA classified it Class II
Apr 7, 2021Published in FDA’s Enforcement Report
Sep 14, 2022FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/63280-hollister-vtad-gastrointestinal-tube-device-recall-risk-of-tube-migration">Hollister VTAD Gastrointestinal Tube Device Recall: Risk of Tube Migration (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1311-2021 (February 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1311-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.