# FDA recall Z-0907-2026

> **C.R. Bard Inc** · Class II · device recall initiated 2025-11-06.

## Product

BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit  REF 788630

## Reason for recall

Labeling discrepancy; Ureteral stent actual size may not match  the actual product label.

## Distribution

Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IA, IN, KY, LA, MA, MD, MI, MO, ND, NJ, NY, OH, PA, SD, VA, WA, WI and the countries of Canada, EMEA (Belgium, Denmark, Slovakia, Spain, Turkey, United Kingdom, MENA (Jordan), S Africa), Greater Asia (China).

## Key facts

- **Recall number:** Z-0907-2026
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-06
- **Report date:** 2025-12-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Covington, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0907-2026

## Citation

> AI Analytics. FDA recall Z-0907-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0907-2026. Source: US FDA. Licensed CC0.

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