Endotrac ECTR Hook Blade — Class II medical device recall Z-2421-2019
Terminated recall by Stryker GmbH, reported 2019-09-04, distributed nationwide. The seal integrity of the sterile bag containing the kits may be compromised.
| Recall number | Z-2421-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, N/A, Switzerland |
| Recall initiated | 2019-07-25 |
| Classified | 2019-08-27 |
| Reported by FDA | 2019-09-04 |
| Terminated | 2020-09-24 |
| Distributed | Nationwide (US) |
| Quantity | 28 |
| Reason classes | sterility, packaging |
| Lot numbers | 01401 |
| Model numbers | 2055A-1 |
Product
Endotrac ECTR Hook Blade, Angled, Catalog Number 2055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.
Reason for recall
The seal integrity of the sterile bag containing the kits may be compromised.
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-2421-2019. 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.