Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0905-2026 — Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614

U.S. FDA — Device Enforcement · United States · 2025-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0905-2026
Date of alert
2025-11-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
C.R. Bard Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741015403
Reported risk: Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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