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.
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.
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.
The tube holder can separate from the barrier that secures the device to the patient's body. This separation might cause the tube to migrate or become lost, potentially leading to injury.
Patients using the VTAD device for gastrointestinal tubes or surgical drains are most at risk. The recall affects specific lot numbers of the model 9782 device.
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.
Look for model number 9782 on the device to confirm if it's affected.
Reach out to Hollister Incorporated for specific instructions on next steps.
The tube holder can separate from the barrier securing the device to the patient's body, which might cause the tube to migrate or become lost, posing a risk of injury.
Check for model number 9782 and lot numbers 0K02, 1A09, or lAlO on the device.
Contact Hollister Incorporated for specific instructions on next steps.
We’ve drafted a message you can send Hollister to request your refund or repair — edit it as you like.
Subject: Recall Z-1311-2021 — Hollister Hollister Hello, I own a Hollister that is covered by recall Z-1311-2021 from Hollister. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
