Neoss 51240 Neoss® Guide - Implant Inserter, Np, Narrow

Recalling firm

Neoss Australia Pty Ltd (NZ)

Product

Neoss 51240 Neoss® Guide - Implant Inserter, NP, Narrow. [Device]. Model: Catalogue number: 51240; Batch 200674 - date of manufacture: 2026-07-27

Reason

The has identified that the guide inserters were produced with incorrect laser marking. The physical product is showing 'S SP'. The correct platform is identified on the product label: 'N NP'. The defect is limited to laser marking only and does not affect the functional characteristics of the device, safety or performance of the instrument if used as intended. The marking is used for device identification only. Based on the technical assessment (CAD/CAM simulation), an NP inserter cannot engage with an SP implant and will rotate in the SP implant., The incorrect laser marking could...

Classification

Class I

Category

medical device recall

Country

New Zealand

Agency

MEDSAFE

Recall date

2026-08-24

Status

Ongoing

Distribution

New Zealand - Healthcare Professional

Official recall notice from MEDSAFE

Recall details on Nibble Recalls: https://trynibble.app/recalls/77d4b6e2-2614-4721-bb9f-b85fa41aac0d