Shippert Medical Technologies recalls Tissu-Trans FILTRON 100 sterile surgical pouches due to potential 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 Tissu-Trans FILTRON 100 sterile surgical pouches because they might have cuts or holes in the pouch that could allow contamination. This could lead to infection or other complications if the pouch isn't properly checked before use.
The pouch may contain hidden cuts or holes that aren't visible without a visual examination. This could compromise the sterile environment needed for medical procedures, increasing the risk of infection or contamination.
Healthcare providers and patients using Tissu-Trans FILTRON 100 sterile surgical pouches for one-time medical procedures are most at risk if the pouch has undetected cuts or holes.
Check the label for Shippert Medical Technologies and the specific lot numbers: 61472, 61601, 61816, 61817, 61818, 61819, 61878, 61736, 61801, 61948, 62050, and 62139.
Visually inspect the pouch for any cuts or holes before use to ensure sterility.
The pouch may contain hidden cuts or holes that aren't visible without a visual examination, which could compromise sterility during medical procedures.
Lot numbers 61472, 61601, 61816, 61817, 61818, 61819, 61878, 61736, 61801, 61948, 62050, and 62139.
Check the label for Shippert Medical Technologies and the specific lot numbers listed above.
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-1330-2019 — Shippert Medical Technologies Shippert Medical Technologies Hello, I own a Shippert Medical Technologies that is covered by recall Z-1330-2019 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.
