Vertical Drain Tube Attachment Device — Class II medical device recall Z-1311-2021
Terminated recall by Hollister Incorporated, reported 2021-04-07, distributed nationwide. The tube holder can separate from the barrier that secures the device to the patients' body. The tube holder h
| Recall number | Z-1311-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hollister Incorporated, Libertyville, IL, United States |
| Recall initiated | 2021-02-11 |
| Classified | 2021-03-26 |
| Reported by FDA | 2021-04-07 |
| Terminated | 2022-09-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| UPC / GTIN / UDI-DI | 00610075097821 |
| Lot numbers | 0K02, 1A09 |
| Model numbers | 9782 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1311-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.