Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number:… — Class II medical device recall Z-2884-2018
Terminated recall by Stryker GmbH, reported 2018-08-29, distributed in KY. Incomplete seal on the Tyvek lid may compromise the sterility of the device
| Recall number | Z-2884-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, Switzerland |
| Recall initiated | 2018-06-27 |
| Classified | 2018-08-22 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2020-04-13 |
| Distributed | KY |
| Quantity | 38 |
| Reason classes | sterility, packaging |
| Lot numbers | 1818-1115S, 1819-1020S, 1819-1220S, 1832-2824S, 1832-2828S, 1832-3826S, K0ACFED, K0B906C, K0BF6C6, K0BF6D2, K0CAEC4, K0CC742 |
| Model numbers | 1818-1115S, 1819-1020S, 1819-1220S, 1832-2824S, 1832-2828S, 1832-3826S, K0ACFED, K0B906C, K0BF6C6, K0BF6D2, K0CAEC4, K0CC742 |
Product
Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S T2 LONG PROXIMAL HUMERAL NAIL LEFT 240mm1832-2824S T2 LONG PROXIMAL HUMERAL NAIL LEFT 280mm 1832-2828S T2 LONG PROXIMAL HUMERAL NAIL RIGHT 260mm 1832-3826S T2 Ankle Arthrd Nail lft 1818-1115S
Reason for recall
Incomplete seal on the Tyvek lid may compromise the sterility of the device
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-2884-2018. 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.