Stradis Healthcare recalls HCT Central Line Insertion Trays (I2 per case) due to potential pinhole leaks in the outer bag that could compromise sterility. Affected units have specific assembly numbers and lot numbers.
Potential for the outer bag having pinhole leaks near the seal, which may result in a breach in the sterility of the kit.
Stradis Healthcare is recalling HCT Central Line Insertion Trays (I2 per case) because the outer bag might have pinhole leaks near the seal. This could breach the sterility of the kit, risking infection during medical procedures.
The outer bag of the tray may develop pinhole leaks near the seal. If these leaks occur, they could compromise the sterility of the medical kit, potentially leading to infections during procedures.
Healthcare professionals using the HCT Central Line Insertion Trays for medical procedures are most at risk. Patients receiving these procedures could be affected if the kit is used without proper sterility.
Check for assembly number HCT8249CP-3 and lot numbers: 222098152, 222551621, 221010141, 222309118, or 222901807. The product was distributed by Health Care Technology.
Verify the assembly number and lot numbers listed in the recall notice to confirm if your unit is affected.
The recall addresses a potential risk of pinhole leaks in the outer bag that could compromise sterility, but the hazard is not described as causing serious injury in normal use.
Check for assembly number HCT8249CP-3 and lot numbers: 222098152, 222551621, 221010141, 222309118, or 222901807.
The recall notice does not specify a remedy, so no action is required beyond checking if your unit is affected.
We’ve drafted a message you can send Strad:is Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0940-2023 — Strad:is Healthcare Strad:is Healthcare Hello, I own a Strad:is Healthcare that is covered by recall Z-0940-2023 from Strad:is 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.
