Home / Brands / Bard Access Systems
Bard Access Systems Recalls
62 recalls on record · September 5, 2012 to July 8, 2026 · Medical Devices
Recalls by year
12
13
14
15
17
18
21
22
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 13, 2013Medical DevicesFDA
Bard Access Systems recalls Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system
Hazard: Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot of Leonard 10.0 French Dual Lumen Catheters with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer Systems due to the wrong size introducer being included with the kit.
September 5, 2012Medical DevicesFDA
Bard Access Systems recalls 16 Fr HemoStar XK Long-Term Hemodialysis Catheter, implanted Standard kit containing an AirGuard introducer. The device
Hazard: Bard Access Systems is recalling one lot of 16 Fr HemoStar XK Long Term Hemodialysis Catheters because they were identified with an incorrect expiration date, 03/2015 rather than 10/2013.