Abbott Vascular Inc: Medical Device Recalls in 2025
Updated on March 25, 2026.
According to to data from the FDA, there were 4 medical device recalls made by Abbott Vascular Inc in 2025. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- 20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices such as balloon dilatation catheters to create and monitor pressure in the balloon.
- 20/30 Priority Pack Accessory Kit/.096 RHV, REF: 1000186, or use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devices).
- 20/30 Priority Pack Accessory Kit w/Copilot, REF: 1003327, used for cardiovascular procedures.
- 20/30 Priority Pack Kit/.115 RHV, REF: 1000186-115, used for cardiovascular procedures.