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.
FDA Recall Z-2673-2016 · Posted None
Recalling FirmNakanishi Inc.
Recall StatusTerminated
Product CodeELC
Date Initiated2016-07-08
Date Terminated2018-06-25
Product Quantity2574 units
Reason for Recall
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.
Firm Action
Naknishi sent out an URGENT : MEDICAL DEVICE CORRECTION letter on July 18, 2016 describing the potential safety issue regarding their Diamond Coated Products. The firm is requesting customers take the following actions:
1. Examine their inventory immediately to determine if they have any product, both used and unused, bearing any of the Nakanishi Product Codes listed in List of Products enclosed with this letter.
2. Immediately dispose of any USED product according to applicable regulations.
3. Segregate any UNUSED product for return to Nakanishi.
4. In order for the firm to complete their records, they are requesting that customers complete the enclosed Correction Activity Sheet and FAX or Mail to:
NSK America, Corp.
1800 Global Parkway, Hoffman Estates, IL 60192 US Facsimile: 1-800-838-9328
Customers with questions were advised to Telephone: 1-888-675-1675.
[email protected]
For questions regarding this recall call 847-843-7664.
Root Cause
Error in labeling
Distribution Pattern
Nationwide Distribution to Illinois, Florida and Georgia.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.