Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0967-2025Class II

Otological Ventilation Tube - T-Tube 12mm - Silicone

Adept Medical Ltd / initiated 2024-11-24 / Open, Classified / root cause: design

Adept Medical Ltd began a recall of Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312 on . FDA classified it as Class II and gives the reason as "Lack of 510(k) clearance". As of , the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number
Z-0967-2025
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
Adept Medical Ltd
Product
Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312;
Product code
ETD Tube, Tympanostomy
Reason for recall
Lack of 510(k) clearance.
Root cause tag
design
FDA root cause
Device Design
Action
On November 25, 2024 distributors were emailed URGENT MEDICAL ADVISORY RECALL NOTICES. We request that you please: 1. Complete the enclosed Recall Acknowledgement Form (even if you have no stock, please confirm via the No Stock tick box). 2. If you have stock, quarantine all stock of the above products. 3. Return the quarantined product to Adept Medical Ltd for credit processing as below. You should also check any stock held elsewhere in your organization. " If returning stock, please return stock with the completed Recall Acknowledgement Form to accompany the returned boxes. " Use our UPS account details as UPS :9F496F , postcode 2022 to process return freight " Send Completed Recall Acknowledgement Form to Yi Huang, Quality and Regulatory Manager, [email protected] and Viv So, Technical File Manager [email protected] We sincerely apologize for the inconvenience caused and assure you that the crediting of your returns will be treated as a matter of utmost urgency.
Quantity in commerce
5,120 units (2190 US, 2930 OUS)
Distribution
US Nationwide distribution. International: Canada, New Zealand, Australia, Yemen, United Kingdom, Spain, Italy, Turkey, El Salvador, Malaysia, United Arab Emirates, Germany, Greece, Syria, Peru, Hong Kong, Turkey, Chile, Ireland.
Product codes and lots
Product Code: NZ3312; UDI-DI: 09421901970383; Lots: 2008-1461, 2011-2537, 2012-2689, 2012-2842, 2015-3945, 2015-4400, 2016-4554, 2016-4662, 2016-5199, 2016-5283, 2017-6007, 2019-6984, 2020-9242, 2020-9690, 2021-10187, 2021-9918, 2023-10966.

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-0967-2025
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-0963-2025Class IIOngoingVoluntary: Firm initiated
Z-0964-2025Class IIOngoingVoluntary: Firm initiated
Z-0965-2025Class IIOngoingVoluntary: Firm initiated
Z-0966-2025Class IIOngoingVoluntary: Firm initiated
Z-0967-2025Class IIOngoingVoluntary: Firm initiated
Z-0968-2025Class IIOngoingVoluntary: Firm initiated
Z-0969-2025Class IIOngoingVoluntary: Firm initiated
Z-0970-2025Class IIOngoingVoluntary: Firm initiated