Medical device recalls Moderate risk

CLINICAL LASERTHERMIA SYSTEMS AB recalls Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Int…

Recall date
April 1, 2021
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1781-2021
FDA classification
Class II
Brand / firm
CLINICAL LASERTHERMIA SYSTEMS AB
Sold / distributed
Worldwide distribution - US Nationwide distribution in the states of TX, MD, CA and the countries of Canada, Germany, Switzerland.

Why it was recalled

single use devices labeled as sterile may not have been adequately sterilized

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Tranberg MR Stylet, 1.8mm/15G, 230mm, REF: 4013-06, Rx Only, Sterile EO - Product Usage: used with the Tranberg¿ MR Introducer; a device used to aid the insertion of the Laser Applicator into the tissue.

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