# FDA recall Z-0787-2021

> **Steris Corporation** · Class II · device recall initiated 2020-12-02.

## Product

Vis-U-All High Temperature Tubing 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs	  Model Number: 881041

## Reason for recall

Purple ink located on the outside label of Vis-U-All Pouches may migrate (bleed) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances, transference of the ink onto the device(s) contained within the pouch

## Distribution

Nationwide  Foreign:

## Key facts

- **Recall number:** Z-0787-2021
- **Recalling firm:** Steris Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-02
- **Report date:** 2021-01-13
- **Termination date:** 2022-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mentor, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0787-2021

## Citation

> AI Analytics. FDA recall Z-0787-2021. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-0787-2021. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*