# FDA recall Z-3094-2026

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2026-07-29.

## Product

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays:  1) KIT,GYN LAPAROSCOPY DH        , Catalog Number: PBOCGLN17

## Reason for recall

The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3094-2026
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-29
- **Report date:** 2026-09-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3094-2026

## Citation

> MORVS. FDA recall Z-3094-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-3094-2026. Source: US FDA. Licensed CC0.

---

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