Recall StatusOpen, Classified
Date Initiated2024-07-31
Product Quantity12,102 reagents
Reason for Recall
Firm identified two lots of reagents that are not meeting the sensitivity statement in the IFU
Firm Action
During the week of 08/15/2024, the firm an "URGENT MEDICAL DEVICE RECALL" Letter via first class mail and/or email. The letter informed customer that Beckman Coulter discovered that IMMAGE Immunochemistry Systems IGM Immunoglobulin M reagent lots are not meeting the sensitivity statement in the IFU: Sensitivity is defined as the lowest measurable concentration which can be distinguished from zero with 95% confidence. Sensitivity for IGM determination is 4.2 mg/dL. .
Customers are instructed to:
-Discontinue use of affected IMMAGE Immunochemistry Systems IGM Immunoglobulin M reagent lots and to follow product replacement instructions.
-Review the Safety Data Sheet (SDS) and discard according to their laboratory's Standard Operating Procedures and/or their local regulations. SDS is available on www.beckmancoulter.com
-Share the content of Recall Letter with their lab and/or medical director regarding the need to perform a retrospective review of patient results.
Beckman Coulter is no longer distributing the affected lots.
For questions, contact Customer Support Center:
. From website: http://www.beckmancoulter.com
. By phone: call 1-800-854-3633 in the United States.
o Outside the United States, contact local Beckman Coulter representative.
. For customers in the United States, if need replacement product:
o Complete the attached Replacement Order Form and email to
[email protected] or fax to (866) 294-7850 OR
o Call Client Services at (800) 526-3821
. For customers in other geographies, contact local Beckman Coulter Representative for replacement.
Distribution Pattern
U.S.: AZ, CA, CO, FL, GA, HI, IL, MA, MI, MO, ND, NY, OH, PA, and TX
O.U.S.: Australia, Belgium, Brazil, Chile, China, Czechia, Ecuador, France, Germany, Greece, Hong Kong, India, Italy, Kuwait, Mexico, Philippines, Poland, Portugal, Saudi Arabia, Slovakia, Spain, Sweden, Taiwan Province of China, and Turkey,
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.