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Recall Observatory FDA recall evidence

Device product

Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2

Z-2488-2023

July 12, 2023

Class II

Product summary

Firm
Beckman Coulter Inc.
Event
Event 92729
Status
Ongoing
Classification
Class II
Quantity
12,850 units
Official record key
device-enforcement:Z-2488-2023

Official wording

Reason: Lipemic interference failed to meet the performance specification listed within the IFU.

Code information: All Lots/UDI-(01)15099590011574

Distribution pattern: US: AL AR AZ CA CO CT DC DE FL GA IA IL IN KS KY LA MA MD MI MN MO MS NC ND NE NJ NM NY OH OK OR PA RI SC SD TN TX UT VA WA WI WV OUS: Algeria, Argentina, Australia, Austria, Bangladesh, Belarus, Belgium, Bosnia and Herzegovina, Brazil, Bulgaria, Canada, China, Colombia, C¿te d'Ivoire, Croatia, Cura¿ao, Cyprus, Czechia, Denmark, Ecuador, Egypt, France, Germany, Gibraltar, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Kazakhstan, Korea, Republic of, Lebanon, Lithuania, Malaysia, Mayotte, Mexico, Morocco, Mozambique, Netherlands, New Zealand, Oman, Pakistan, Philippines, Poland, Portugal, Puerto Rico, Qatar, Romania, Russian Federation, San Marino, Saudi Arabia, Serbia, Singapore, Slovakia, South Africa, Spain, Switzerland, Taiwan, Province of China, Tunisia, Turkey, United Arab Emirates, United Kingdom of Great Britain and Northern Ireland, Uruguay, Viet Nam, Yemen.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Lipemic interference failed to meet the performance specification listed within the IFU.