Merit Medical Systems, Inc. Merit Medical systems, Inc, Convenience Kit REF/CAT no.: K09-07692 REVISION A , CUSTOM KIT Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Merit Medical systems, Inc, Convenience Kit REF/CAT no.: K09-07692 REVISION A , CUSTOM KIT
Brand
Merit Medical Systems, Inc.
Lot Codes / Batch Numbers
Lot #F726849
Products Sold
Lot #F726849
Merit Medical Systems, Inc. is recalling Merit Medical systems, Inc, Convenience Kit REF/CAT no.: K09-07692 REVISION A , CUSTOM KIT due to Potential sterility breach caused by excessive shipment damage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential sterility breach caused by excessive shipment damage.
Recommended Action
Per FDA guidance
Merit Medical Customers were contacted directly by phone and letter on 9/29/09. Customers were instructed to identify and quarantine all unused affected product. Further information was available at 801-208-4365.
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
AL, GA, KY, LA, MO, OR, TN
Page updated: Jan 10, 2026