Official recall record
PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-07-17
- Country of alert
- Germany
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 15099590673567
- Brand on record
- Beckman Coulter Biomedical GmbH
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Other recalls from this brand
- 2024-07-17 · US FDA — Medical Devices
Power Express, REF B90918
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