Abbott Vascular recalls 20/30 Priority Pack Accessory Kits with potential leaks and loose connections. Affected units include specific part numbers and lot numbers from 2019. Contact for remedy details.
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Abbott Vascular is recalling two types of 20/30 Priority Pack Accessory Kits due to reported leaks and intermittent/loose connections. This could lead to improper medical use if the kits fail during procedures.
The kits have been reported to leak or have loose connections, which could cause improper medical procedures if the connections fail during use. This is a potential issue for medical devices used in critical situations.
Medical professionals using these kits during procedures are most at risk. Patients receiving these kits may be affected if the connections fail during treatment.
Check for part numbers 1000186 or 1000186-115, and lot numbers listed in the recall notice (e.g., 60317536, 60320079). These kits were sold starting March 1, 2019.
Verify your kit's part number and lot number against the list provided in the recall notice.
The recall states there have been complaints about leaks and loose connections, but the kits are not yet unsafe for use. Affected units should be checked and replaced.
Check for part numbers 1000186 or 1000186-115 and lot numbers like 60317536, 60320079, or others listed in the recall notice.
The recall does not specify a remedy, so contact Abbott Vascular directly for further instructions.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0922-2022 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0922-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.