Beckman Coulter IRISPEC CA/CB/CC Urine Chemistry Controls, Catalog Number REF 800-7211 and 800-7702, in vitro diagnostic device.
FDA Recall Z-0093-2025 · Posted 2024-10-16
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Recalling FirmBeckman Coulter, Inc.
Recall StatusOpen, Classified
Product CodeJJW
Date Initiated2024-07-16
Product Quantity5589 units
Reason for Recall
Beckman Coulter has become aware of an increase in customer complaints for intermittent IRISpec CB negative glucose control failure, resulting in false positive control results when used in conjunction with iChemVELOCITY Urine Chemistry Strips (PNs 800-7204 and 800-7212) on the iChemVELOCITY Analyzer. This issue may delay the reporting of patient results, with a worst-case scenario of a delay in diagnosis or treatment of metabolic disorders, kidney function abnormalities, urinary tract infections, and liver function.
Firm Action
Beckman Coulter issued an URGENT MEDICAL DEVICE RECALL notice to its consignees beginning on 07/15/2024 by letter delivered by either USPS first class mail or email. The notice explained the issue, potential impact, and provided updated QC ranges for Glucose in the Analyzer. The information is to be shared with all affected parties.
For questions: please contact Customer Support Center or your local representative;
From our website: http://www.beckmancoulter.com
By phone: Call 800-526-7694 in the United States and Canada.
o Outside the United States and Canada, contact your local Beckman Coulter
representative.
Root Cause
Under Investigation by firm
Distribution Pattern
worldwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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