Atlas FDA

Merit Medical systems, Inc, Convenience Kit REF/CAT no.: K09-07692 REVISION A , CUSTOM KIT

FDA device recall Z-0524-2010 · posted 2009-12-14 · Terminated

Recall details

Recalling firm
Merit Medical Systems, Inc.
Reason for recall
Potential sterility breach caused by excessive shipment damage.
Action taken
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.
Root cause
Other
Status
Terminated
Product code
MDM
Quantity affected
30 kits
Distribution
US (AL, LA, MO, KY, TN, GA). No military, government or foreign distribution.
Date initiated
2009-09-29
Date posted
2009-12-14
Date terminated
2009-12-15
Location
South Jordan, UT

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