Bard Poly Midline Catheter Recall
Bard Access Systems is recalling Poly Midline Catheters (models CK000495A and CK000566) because the lidocaine supplied with these catheters was made under …
Bard Access Systems, Inc.
Bard Access Systems, Inc. Recalls (2026)
Every recall we are tracking for Bard Access Systems, Inc., newest first, sourced from the FDA. If you are wondering whether your Bard Access Systems, Inc. product is recalled in 2026, check the list below for your model, lot, or VIN. Each entry explains the hazard and the free repair, replacement, or refund. Get a free email alert the moment a new Bard Access Systems, Inc. recall posts.
1 recall · updated May 21, 2026
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