# FDA recall Z-0807-2021

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2020-12-11.

## Product

VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.

## Reason for recall

VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.

## Distribution

Worldwide distribution - US Nationwide distribution including in the states of FL, IL, MA, MS, OH, OR, TX, VA, WA, WV and the countries of Australia, Poland, and United Kingdom.

## Key facts

- **Recall number:** Z-0807-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-11
- **Report date:** 2021-01-20
- **Termination date:** 2023-03-24

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0807-2021

## Citation

> AI Analytics. FDA recall Z-0807-2021. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-0807-2021. Source: US FDA. Licensed CC0.

---

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