Merit Medical Systems, Inc Merit Custom Procedure Kit Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Merit Custom Procedure Kit
Brand
Merit Medical Systems, Inc
Lot Codes / Batch Numbers
Part Number: K08-01894, Lot Number A306856
Products Sold
Part Number: K08-01894, Lot Number A306856
Merit Medical Systems, Inc is recalling Merit Custom Procedure Kit due to Component of procedure kits may allow higher than desired amount of IV solution to be infused in to patient during pressure monitoring procedure.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Component of procedure kits may allow higher than desired amount of IV solution to be infused in to patient during pressure monitoring procedure.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 9/2/2005.
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
MD, OR, VA, DC
Page updated: Jan 10, 2026