Dual Articulating Headrest — Class II medical device recall Z-0984-2024
Ongoing recall by Steris Corporation, reported 2024-02-14, distributed nationwide. Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure
| Recall number | Z-0984-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Steris Corporation, Mentor, OH, United States |
| Recall initiated | 2023-12-12 |
| Classified | 2024-02-05 |
| Reported by FDA | 2024-02-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, MX, NZ |
| Quantity | 80 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00724995195885 |
| Model numbers | BF753 |
Product
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Reason for recall
Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay.
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-0984-2024. 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.