All recalls
FDA
Food and Drug Administration · Recall Z-2656-2026 · May 21, 2026

CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 The Poly Per-Q-Cath Midline catheters are indicated for short or lon

Bard Access Systems, Inc.

The hazard

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

The remedy

Follow FDA guidance

About this recall

CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108051 The Poly Per-Q-Cath Midline catheters are indicated for short or long term peripheral access to the peripheral venous system for selected intravenous therapies and blood sarnpling.

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

UPC 00801741121609UPC 00801741108051

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.