Abbott Vascular recalls 20/30 Priority Pack w/COPILOT devices from 2019 with leaks and intermittent connections. Affected units include specific lot numbers and part numbers.
Due to an increase in complaint trend for leaks and intermittent/loose connections.
Abbott Vascular is recalling 20/30 Priority Pack devices with COPILOT that have reported leaks and loose connections. This could lead to improper function during medical procedures.
The devices have experienced leaks and intermittent/loose connections due to increased complaints. This could cause improper function during medical procedures, but the risk is not severe enough to cause serious injury.
Medical device users who own the recalled 20/30 Priority Pack w/COPILOT models from 2019. Patients and healthcare providers using these devices are most at risk.
Check for the product name '20/30 Priority Pack w/COPILOT', part number 1003327, or lot numbers listed in the recall notice. The devices were sold starting March 1, 2019.
Look for the part number 1003327 or lot numbers listed in the recall notice to confirm if your device is affected.
Abbott Vascular is recalling these devices due to increased complaints about leaks and intermittent/loose connections.
Check the part number and lot numbers listed in the recall notice to see if your device is affected. If it is, contact Abbott Vascular for further instructions.
The recall is due to leaks and loose connections, which could cause improper function during medical procedures, but the risk is not severe enough to cause serious injury.
We’ve drafted a message you can send Abbott Vascular to request your refund or repair — edit it as you like.
Subject: Recall Z-0923-2022 — Abbott Vascular Abbott Vascular Hello, I own a Abbott Vascular that is covered by recall Z-0923-2022 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.
