# FDA recall Z-1311-2021

> **Hollister Incorporated** · Class II · device recall initiated 2021-02-11.

## 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.

## Reason for recall

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.

## 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 of Canada.

## Key facts

- **Recall number:** Z-1311-2021
- **Recalling firm:** Hollister Incorporated
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-02-11
- **Report date:** 2021-04-07
- **Termination date:** 2022-09-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Libertyville, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1311-2021

## Citation

> AI Analytics. FDA recall Z-1311-2021. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1311-2021. Source: US FDA. Licensed CC0.

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