Instrumentation Laboratory Co. Instrumentation Laboratory ACL TOP Coagulation Analyzer (Base Model only). Blood analyzer. P/N 280000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Instrumentation Laboratory ACL TOP Coagulation Analyzer (Base Model only). Blood analyzer. P/N 280000
Brand
Instrumentation Laboratory Co.
Lot Codes / Batch Numbers
Serial numbers prior to 07060782
Products Sold
Serial numbers prior to 07060782
Instrumentation Laboratory Co. is recalling Instrumentation Laboratory ACL TOP Coagulation Analyzer (Base Model only). Blood analyzer. P/N 2800 due to ACL TOP unit, when in emergency stop may release liquid during recovery sequence and contaminate sample tube.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
ACL TOP unit, when in emergency stop may release liquid during recovery sequence and contaminate sample tube.
Recommended Action
Per FDA guidance
Instrumentation Laboratory notiifed the distributor Beckman Coulter on 6/19/2007. Beckman Coulter notified their customers and provided a copy with the Instructions for Recovery Procedure on how to avoid contamination from probe leaks.
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 noticePage updated: Jan 10, 2026