Abbott Vascular Inc FDA Recalls

4 recalls on file across devices, 0 of them Class I and 4 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular procedures in conjunction with intervenClass IINov 6, 2024Inflation Device used during cardiovascular procedures may l	Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or	Class IIDevices	Nov 6, 2024
20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular procedures.Class IINov 6, 2024Inflation Device used during cardiovascular procedures may l	Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or	Class IIDevices	Nov 6, 2024
20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices suchClass IINov 6, 2024Inflation Device used during cardiovascular procedures may l	Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or	Class IIDevices	Nov 6, 2024
20/30 Priority Pack Kit/.115 RHV, REF: 1000186-115, used for cardiovascular procedures.Class IINov 6, 2024Inflation Device used during cardiovascular procedures may l	Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or	Class IIDevices	Nov 6, 2024