FDA Device recall Z-0984-2024
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
- FDA Device
- Class II
- ongoing
- Published 2024-02-14
On 2024-02-14 the FDA classified a Class II recall of Dual Articulating Headrest, Velcro P/N P141210813, REF BF753 by Steris, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0984-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-12-12 |
| Published | 2024-02-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Steris |
| Distribution | US |
Product
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Reason
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.
Identifiers
| code_info | UDI-DI: 00724995195885, date of manufacture 2023-08-14 thru 2023-10-26. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0984-2024%22
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