FDA Device recall Z-0223-2019
Micro Surgery Handpiece SGS, Model: SGS-ES, Order Code: H264, Manufactured by: Nakanishi Inc
- FDA Device
- Class II
- terminated
- Published 2018-10-31
On 2018-10-31 the FDA classified a Class II recall of Micro Surgery Handpiece SGS, Model: SGS-ES, Order Code: H264, Manufactured by: Nakanishi Inc by Nakanishi, citing reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previ….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0223-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-01 |
| Published | 2018-10-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Nakanishi |
| Distribution | CA, FL, GA, IL, WA |
Product
Micro Surgery Handpiece SGS, Model: SGS-ES, Order Code: H264, Manufactured by: Nakanishi Inc. The SGS/SGA Surgical Handpieces are intended for surgical use. Typical usage includes dental implant use: drilling and tapping the maxilla and mandible.
Reason
Reprocessing instructions for the SGS/SGA Surgical Handpieces have been updated with instructions of manual cleaning and specific parameters for autoclave sterilization. The previous operation manuals associated with the SGS/SGA products must be replaced by new operation manuals.
Identifiers
| code_info | Previous Operation Manuals: OM-SH0015E002,OM-SH0015E003, OM-SH0015E004, OM-SH0015E005, OM-SH0100F, OM-SH0096S Model…Previous Operation Manuals: OM-SH0015E002,OM-SH0015E003, OM-SH0015E004, OM-SH0015E005, OM-SH0100F, OM-SH0096S Model Name: SGS-ES; Order Code H264/H264007 Serial Nos.:0LZ00063 - 0LZ00064, 0LZ00066 - 0LZ00068, 0LZ00070 - 0LZ00109; 0LZ00110 - 0LZ00115; 0BB20112 -0BB20116, 0BB20226 - 0BB20229, 0BB40071 - 0BB40075, 0BB50186 - 0BB50189, 0BB50215 - 0BB50224, 0BB50263, 0BB50265, 0BB50266, 0BB50185, 0BB50190 - 0BB50192; 0BB60051 - 0BB60055, 0BB60079 - 0BB60100, 0BB60106 -0BB60118, 0BB70066 - 0BB70100, 0BB90004 - 0BB90058, 0BB90123 - 0BB90132, 0BBX0168 - 0BBX0175;0BBY0188 -0BBY0192; 0BC10095 - 0BC10099, 0BC10101 - 0BC10110, 0BC10121 - 0BC10130, 0BC10169 - 0BC10170, 0BC10176- 0BC10179, 0BC50093 - 0BC50102, 0BC60001 - 0BC60040, 0BC60085 - 0BC60104, 0BC60078 - 0BC60081, 0BC90001 - 0BC90090; 0BCY0003 - 0BCY0032; 0BD40011 -0BD40020, 0BD60001 - 0BD60034, 0BD60008 - 0BD60010, 0BD60016, 0BD60142-0BD60150, 0BD70062-0BD70072, 0BD80001 -0BD80034, 0BD80095 - 0BD80100, 0BDX0021 -0BDX0040, 0BD |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0223-2019%22
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