FDA Device recall Z-2980-2024
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express
- FDA Device
- Class II
- ongoing
- Published 2024-09-11
On 2024-09-11 the FDA classified a Class II recall of PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express by Beckman Coulter Biomedical, citing the adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This deta….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2980-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-07-17 |
| Published | 2024-09-11 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Beckman Coulter Biomedical |
| Distribution | US |
Product
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
Reason
The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
Identifiers
| code_info | UDI: (01)15099590673567/ All serial numbers |
|---|
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-2980-2024%22
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