Bard Access Systems, Inc. recalls
2 recalls on record · FDA
Every recall we have on record for Bard Access Systems, Inc., compiled from federal safety data. Check the hazard, the remedy, and how serious each one is, and always confirm on the official notice.
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Health Serious
CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 …
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, Inc. Jul 8, 2026
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Health Serious
5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Bard Access Systems, Inc. Jul 8, 2026
Read the recall