Harvard Clinical Technology Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N 2002-001) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N 2002-001)
Brand
Harvard Clinical Technology
Lot Codes / Batch Numbers
Software versions V1.2R or earlier
Products Sold
Software versions V1.2R or earlier
Harvard Clinical Technology is recalling Software Versions V1.2R,or earlier for the Harvard 2, Dual Infusion Pump (P/N 2002-001) due to Under specific sequence conditions, the unit may apper to be infusing, but is not. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Under specific sequence conditions, the unit may apper to be infusing, but is not
Recommended Action
Per FDA guidance
Harvard Medical Technology inc. notified customers by letter on 8/11/03, advising users of the software upgrade to version V1.3T. Facilities will be visited by technicians who will upgrade the software.
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