---
title: "BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit ... — FDA record Z-0906-2026 | Is It on Recall"
description: "Labeling discrepancy; Ureteral stent actual size may not match the actual product label."
url: https://isitonrecall.com/recall/fda-device-z-0906-2026-bd-inlay-optima-ureteral-stent-kit-size-4-7-fr-x-26-cm-ureteral-stent-kit-ref-788426/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426 — FDA record Z-0906-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 6, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
- **Reason**: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- **Classification**: Class II
- **Recalling firm**: C.R. Bard Inc
- **Quantity**: 4350 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0906-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0906-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot# NGJU4181/UDI: (01)00801741015687 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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).

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Dec 17, 2025
- **Recall initiation date**: Nov 6, 2025
- **Center classification date**: Dec 11, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0906-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [C.R. Bard Inc records](https://isitonrecall.com/brand/c-r-bard-inc/)
