Smiths Medical MD, Inc. Smiths Medical CADD-Sentry Pro Medication Safety Software - electronic pump protocol programming software - Administrator REF 21-6275-51 RX only, Smiths Medical MD, Inc. St Paul, Minnesota 55112 USA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Smiths Medical CADD-Sentry Pro Medication Safety Software - electronic pump protocol programming software - Administrator REF 21-6275-51 RX only, Smiths Medical MD, Inc. St Paul, Minnesota 55112 USA
Brand
Smiths Medical MD, Inc.
Lot Codes / Batch Numbers
Catalog Number: 21-6275-51, Software Version B.
Products Sold
Catalog Number: 21-6275-51, Software Version B.
Smiths Medical MD, Inc. is recalling Smiths Medical CADD-Sentry Pro Medication Safety Software - electronic pump protocol programming sof due to Incorrect dosage possible: A software anomaly in the CADD-Sentry Pro Administrator software (version B) where the values of a weight based protocol go. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect dosage possible: A software anomaly in the CADD-Sentry Pro Administrator software (version B) where the values of a weight based protocol go to zero or round up to the next higher hundredths place, even if Administrator displayed the values correctly at data entry.
Recommended Action
Per FDA guidance
A Smiths Medical MD employee visited the consignees between August 14 and 31, 2007, to verbally notify them of the recall, collect the recall CD-ROM containing the affected software and replace with the updated 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 noticeDistribution
As reported by FDA
CO, MD, UT
Page updated: Jan 10, 2026