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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.
See this for other years:
2014
2025
  • 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.
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