Data Foundry

Medical device recalls 2025

Otological Ventilation Tube — Class II medical device recall Z-0967-2025

Ongoing recall by Adept Medical Ltd, reported 2025-01-29, distributed nationwide. Lack of 510(k) clearance.

Recall numberZ-0967-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmAdept Medical Ltd, Auckland, New Zealand
Recall initiated2024-11-24
Classified2025-01-17
Reported by FDA2025-01-29
DistributedNationwide (US)
Countries outside the USAE, AU, CA, CL, DE, ES, GB, GR, HK, IE, IT, MY, NZ, PE, SV, TR
UPC / GTIN / UDI-DI09421901970383
Lot numbers2008-1461, 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

Product

Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312;

Reason for recall

Lack of 510(k) clearance.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0967-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.