Home / Brands / Bard Medical Division
Bard Medical Division Recalls
5 recalls on record · August 1, 2018 to May 8, 2019 · Medical Devices
Recalls by year
18
19
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 8, 2019Medical DevicesFDA
Bard Medical Division recalls Medivance(R) ARCTIC SUN(R) ARCTICGEL(TM) Pads: Description, Catalog Number a) Intrepid ArcticGel Small Pad Kit, 31705I
Hazard: Specific lots of ArcticGel Pads have potential issues which may result in the insufficient adhesion of the hydrogel to the pad.
February 13, 2019Medical DevicesFDA
Bard Medical Division recalls SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A11
Hazard: potential for urine leakage around the vent on the vented sample port
February 13, 2019Medical DevicesFDA
Bard Medical Division recalls BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with Bard
Hazard: Some SureStep" Foley Tray Systems with product catalog number A319418AM and lot number NGCT1929 contain vented sample ports that may have an increased likelihood of leaking urine from the vent on the sample port.
September 5, 2018Medical DevicesFDA
Bard Medical Division recalls Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads a
Hazard: Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads were not meeting the iodine assay level requirements to support 36 month expiration dating.
August 1, 2018Medical DevicesFDA
Bard Medical Division recalls Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulati
Hazard: An improper wiring connection on the chiller assembly may result in overheating of the connection and potential failure of certain components in the system.