Abbott Vascular recalls 20/30 INDEFLATORS (ref 1000184) used in cardiovascular procedures due to potential air embolism from leaks at hose connections. Affected units have specific UDI-DI and lot numbers.
Inflation Device used during cardiovascular procedures may leak in the indeflator at the hose rotating luer or at the gauge, which could lead to air embolism.
Abbott Vascular is recalling 20/30 INDEFLATORS used in cardiovascular procedures because they may leak air at hose connections, risking air embolism. This could cause serious complications during medical procedures.
The inflation device may leak air at the hose rotating luer or gauge during use. This air could enter the bloodstream, causing air embolism which can lead to serious complications like stroke or organ damage.
Healthcare professionals using these devices during cardiovascular procedures are most at risk. Patients undergoing such procedures with the recalled equipment could be affected.
Check for the product name '20/30 INDEFLATOR' with reference number 1000184. Affected units have UDI-DI: 08717648013591 and lots 60418466, 60418467, or 60418468.
Identify the UDI-DI number (08717648013591) and lot numbers (60418466, 60418467, 60418468) to confirm if your device is affected.
The 20/30 INDEFLATOR may leak air at hose connections during use, which could lead to air embolism in patients during cardiovascular procedures.
Check the UDI-DI number and lot numbers to see if your device is affected. If it is, contact Abbott Vascular for further instructions.
Yes, air embolism can cause serious complications like stroke or organ damage if air enters the bloodstream during procedures.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0730-2025 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0730-2025 from Abbott Vascular. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
