Beckman Coulter Inc.: Medical Device Recall in 2017 - (Recall #: Z-1833-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Access Ferritin Calibrators, Part No. 33025, Ref No. B50136C

Product Classification:

Class II

Date Initiated: March 10, 2017

Date Posted: April 26, 2017

Recall Number: Z-1833-2017

Event ID: 76838

Reason for Recall:

Beckman Coulter is recalling the Access Ferritin Calibrators kit because it contains a calibration card with an incorrect S5 calibrator concentration.

Status: Terminated

Product Quantity: 889 kits total (6 kits in US)

Code Information:

Lot No. 671094

Distribution Pattern:

Worldwide Distribution - US Distribution and to the countries of : Algeria, Bangladesh, Belgium, Botswana, Croatia, Czech Republic, Denmark, Djibouti, Egypt, France, Germany, Ghana, Greece, Hungary, Ireland, Italy, Kazakhstan, Lebanon, Lithuania, Morocco, Nepal, Netherlands, Oman, Pakistan, Poland, Portugal, Romania, Russia, Saudi Arabia, Slovakia, South Africa, Spain, Sweden, Switzerland, Turkey, United Kingdom, and Zimbabwe.

Voluntary or Mandated:

Voluntary: Firm initiated