Abbott Laboratories Abbott CELL-DYN 3000 Hematology Analyzer Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Abbott CELL-DYN 3000 Hematology Analyzer
Brand
Abbott Laboratories
Lot Codes / Batch Numbers
Model number CELL-DYN 3000 CS: List Numbers 91323-01 and 91323-03, all serial numbers distributed on or before May 3, 2007. Model number CELL-DYN 3000 SL: List Numbers 91325-01 and 91325-03, all serial numbers distributed on or before May 3, 2007.
Products Sold
Model number CELL-DYN 3000 CS: List Numbers 91323-01 and 91323-03, all serial numbers distributed on or before May 3, 2007. Model number CELL-DYN 3000 SL: List Numbers 91325-01 and 91325-03; all serial numbers distributed on or before May 3, 2007.
Abbott Laboratories is recalling Abbott CELL-DYN 3000 Hematology Analyzer due to The product failed electrostatic discharge testing, which could result in product failure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product failed electrostatic discharge testing, which could result in product failure.
Recommended Action
Per FDA guidance
Mandatory Technical Service Bulletins (TSB) are being issued to Field Service to upgrade all instruments in the field. All customers will be contacted by Field Service to schedule this mandatory upgrade. The upgrades are expected to take 12 months.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
PR
Page updated: Jan 10, 2026