Medical device recalls Moderate risk

Nakanishi product recalled over sterility concerns

Recall date
July 8, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Nakanishi Inc. recalls Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The inten…
Recall number
Z-2673-2016
FDA classification
Class II
Brand / firm
Nakanishi Inc.
Sold / distributed
Nationwide Distribution to Illinois, Florida and Georgia.

Why it was recalled

Through an error, the labeling failed to include the symbol or other text indicating that the diamond coated tips were single use only. A contributing factor to this error is that in other markets such as Japan, the diamond coated tips are multiple use and are not limited to single use only. The tips are stainless steel with a coating of fine diamond powder. The tips are sold non-sterile and are to be sterilized prior to first use. The tips were cleared as single use only. This problem was discovered during an ongoing, proactive, quality system improvement plan that was initiated by Nakanishi in October 2014. Because the correct instructions for sterilization are not available, it is possible that the devices might not be sterile prior to use. The absence of the single use statement introduces a risk of cross-contamination if the tips are reprocessed and reused.

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

What was recalled

Diamond Coated Tips and Burs are accessories to the air powered Bone drill (VARIOSURG with and without light) The intended use of the tips is based on the parent device. For the VarioSurg, in addition to the scaling functions, diamond coated tips are used for socket lift, sinus lift, and implant preparation.

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