Stradis Healthcare recalls Vas Pack item 888-2520 due to potential sterility breaches from incomplete bag sealing. Affected kits may not be sterile, risking infection during medical procedures.
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling Vas Pack medical kits because manufacturing issues could cause the outer bag to be incompletely sealed. This might breach the sterility of the kit, increasing infection risk during medical procedures.
The manufacturing process may leave the outer bag of the medical kit incompletely sealed. This could allow contamination, breaking the sterility of the kit and potentially causing infections during medical procedures.
Healthcare professionals using the Vas Pack kits for medical procedures are most at risk. Patients receiving these kits could face infection if the sterility is compromised.
Check for the Vas Pack item number 888-2520 on the product. The UDI/DI (case) is H65888825201 and UDI/DI (kit) is M75288825200. Serial/Lot Numbers start with 22256490684.
Identify the Vas Pack item 888-2520 with UDI/DI (case) H65888825201 and UDI/DI (kit) M75288825200.
The manufacturing process may result in the outer bag being incompletely sealed, which could breach the sterility of the medical kit.
If the sterility is compromised, it could lead to infection during medical procedures.
Look for the Vas Pack item number 888-2520 with UDI/DI (case) H65888825201 and UDI/DI (kit) M75288825200.
We’ve drafted a message you can send Stradis Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0556-2023 — Stradis Healthcare Stradis Healthcare Hello, I own a Stradis Healthcare that is covered by recall Z-0556-2023 from Stradis Healthcare. 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.
