5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: recall status

⚠ Recall found. 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code is named in 1 official recall in our current data. Details and the official notices are below — act on the remedy in the official notice.

Brand: Bard Access Systems

Recalls naming this model

FDA Class II · Medical device · July 8, 2026

5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code recall — Bard Access Systems, Inc.

Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

Official ID Z-2657-2026 · Official record ↗

See all Bard Access Systems recalls →

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FDA — food, drugs, medical devices ↗ (aggregated here)
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Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:09 AM UTC.