CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg Laser Applicators with lot numbers 00247/2019/11, 00029/2020/02, 00076/2020/03, 00177/2018/10-1, 00177/2018/10-2, 00049/2020/02. These single-use devices labeled as sterile may not have been adequately sterilized.
single use devices labeled as sterile may not have been adequately sterilized
CLINICAL LASERTHERMIA SYSTEMS AB is recalling Tranberg Laser Applicators that may not have been properly sterilized. This could lead to infections if used in medical procedures. The recalled items are single-use devices labeled as sterile.
Single-use devices labeled as sterile may not have been adequately sterilized. This means they could become contaminated and cause infections during medical procedures. The hazard is specific to devices that are intended for one-time use only.
Healthcare providers who use these laser applicators for medical procedures are most at risk. Patients receiving treatments with these devices could be affected if the devices were not properly sterilized.
Check for the lot numbers: 00247/2019/11, 00029/2020/02, 00076/2020/03, 00177/2018/10-1, 00177/2018/10-2, or 00049/2020/02. These are the specific lots of Tranberg Laser Applicators that are recalled.
Look for the lot numbers listed: 00247/2019/11, 00029/2020/02, 00076/2020/03, 00177/2018/10-1, 00177/2018/10-2, or 00049/2020/02.
The recall states that single-use devices labeled as sterile may not have been adequately sterilized. If you have one of the recalled lot numbers, it is not safe to use.
Check the lot number on your device. If it matches the recalled lots, contact CLINICAL LASERTHERMIA SYSTEMS AB for instructions.
Look for the lot numbers: 00247/2019/11, 00029/2020/02, 00076/2020/03, 00177/2018/10-1, 00177/2018/10-2, or 00049/2020/02.
We’ve drafted a message you can send Tranberg to request your refund or repair — edit it as you like.
Subject: Recall Z-1782-2021 — Tranberg Tranberg Hello, I own a Tranberg that is covered by recall Z-1782-2021 from Tranberg. 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.
