Every recall we track for CLINICAL LASERTHERMIA SYSTEMS AB — 3 in all — plus the complaints and injury reports the public filed about them.
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.
CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Cannula (REF 401:05) due to potential inadequate sterilization of single-use sterile devices. This affects medical devices used with the Tranberg MR Introducer for laser tissue procedures.
CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Stylets (REF: 4013-06) due to potential inadequate sterilization. These single-use sterile devices may not be properly sterilized, risking infection.
