Shippert Medical Technologies recalls sterile Tissu-Trans FILTRON 250 products with possible pouch cuts or holes 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 sterile Tissu-Trans FILTRON 250 medical products due to potential cuts or holes in the pouch that could compromise sterility. This risk means the products might not be sterile when used, which could lead to infections.
The pouch may have cuts or holes that aren't visible without a visual examination. This could mean the product isn't sterile when used, potentially causing infections in patients during medical procedures.
Healthcare providers and patients using the Tissu-Trans FILTRON 250 for one-time medical procedures are affected. Patients with specific medical conditions requiring sterile procedures may be at higher risk.
Check for the product name 'Tissu-Trans FILTRON 250' and catalog number 3-TT-FILTRON 250. Look for lot numbers 61507, 61578, 61682, 61689, 61849, 61879, 62011, 62088, or 62108 on the label.
Look for the lot numbers 61507, 61578, 61682, 61689, 61849, 61879, 62011, 62088, or 62108 on the product label.
The product may have cuts or holes in the pouch that aren't visible without a visual examination, so it might not be sterile when used. Do not use if you find any cuts or holes.
Check the product label for the lot numbers listed. If you have the listed lot numbers, stop using it and contact Shippert Medical Technologies for instructions.
Look for the product name 'Tissu-Trans FILTRON 250' and catalog number 3-TT-FILTRON 250 with lot numbers 61507, 61578, 61682, 61689, 61849, 61879, 62011, 62088, or 62108 on the label.
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-1331-2019 — Shippert Medical Technologies Shippert Medical Technologies Hello, I own a Shippert Medical Technologies that is covered by recall Z-1331-2019 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.
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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.
