FDAOctober 31, 2016device

CADD Solis VIP Ambulatory Infusion Pump, Model 21-21210, Reorder 21-2120-0102-15,

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

20 Pumps sold to the Finnish market contain a message in which one word in the message is mistranslated. When the user follows a specific set of key presses the pump will display the incorrect message. The message indicates that a Patient Controlled Analgesia (PCA) dose is unavailable because the pump is running. It should indicate that the PCA dose is not available because the pump is stopped. The function of the pump is unchanged and no patient injury can occur since no drug is being delivered.

What to do

FDA enforcement status: Terminated

Brands named

smiths medical asdsmithssmiths medical

UPCs

212120010215

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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