Shippert Medical Technologies recalls Tissu-Trans MEGA 1500 sterile medical pouches due to potential cuts or holes in pouches that could compromise sterility during use.
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 sterile medical pouches because they might have cuts or holes that could let contaminants in. This could lead to infections if the pouch isn't checked properly before use.
The pouch might have cuts or holes that aren't visible without a visual examination. This could allow contaminants to enter the sterile product, increasing infection risk during medical procedures.
Patients using this sterile medical pouch for one-time procedures are most at risk if the pouch has cuts or holes that compromise sterility. Healthcare providers who use these products should check pouch integrity before each use.
Check for the label with 'Shippert Medical Technologies' and catalog number 3-TT-MEGA 1500. The product is a sterile, disposable, one-patient use pouch sold in specific zip codes.
Visually inspect the pouch for cuts or holes before use to ensure sterility.
The product may have cuts or holes that could compromise sterility, so it's not safe to use without visual inspection.
Look for the label with 'Shippert Medical Technologies' and catalog number 3-TT-MEGA 1500, sold in specific zip codes.
Visually inspect the pouch for cuts or holes before use; if you find any, do not use it.
We’ve drafted a message you can send Shippert Medical Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1335-2019 — Shippert Medical Technologies Shippert Medical Technologies Hello, I own a Shippert Medical Technologies that is covered by recall Z-1335-2019 from Shippert Medical Technologies. 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.
