Instrument Tray — Class II medical device recall Z-0980-2019
Terminated recall by Stryker GmbH, reported 2019-03-13. The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.
| Recall number | Z-0980-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, N/A, Switzerland |
| Recall initiated | 2019-01-21 |
| Classified | 2019-03-06 |
| Reported by FDA | 2019-03-13 |
| Terminated | 2020-04-02 |
| Countries outside the US | CA, KR |
| Quantity | 17 units |
| Lot numbers | K026ACE |
| Model numbers | 1806-9900 |
Product
Instrument Tray, Basic T2 Femur Long Catalog #: 1806-9900 Product Usage: Knee Arthroplasty
Reason for recall
The faceplates may incorrectly identify the T2 Basic Long Instrument Set as T2 Basic Short Instrument Set.
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-0980-2019. 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.