Beckman Coulter Biomedical GmbH: Medical Device Recall in 2024 - (Recall #: Z-2980-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.

Product Classification:

Class II

Date Initiated: July 17, 2024

Date Posted: September 11, 2024

Recall Number: Z-2980-2024

Event ID: 95064

Reason for Recall:

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.

Status: Ongoing

Product Quantity:

Code Information:

UDI: (01)15099590673567/ All serial numbers

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Australia, Bahrain, Canada, China, Colombia, Egypt, France, Germany, Italy, Jordan, Korea, Kuwait, Lebanon, Malaysia, Panama, Qatar, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, Thailand, Turkey, United Arab Amirates, United Kingdom, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated