Atlas FDA

Custom Kit, Cardiac Cath Kit, Rx only, REF/CAT No.: K09-90240HP, Merit Medical Systems, South Jordan, Utah.

FDA device recall Z-0846-2007 · posted 2007-05-31 · Terminated

Recall details

Recalling firm
Merit Medical Systems, Inc.
Reason for recall
Male luer in fluid administration sets may crack due to inadequate molding process
Action taken
Consignees were notified by letter on 04/17/2007 and instructed to quarantine and return any unused product.
Root cause
Other
Status
Terminated
Product code
FMG
Quantity affected
717 units
Distribution
CA, IL, NJ, NY. No military, government or foreign distribution.
Date initiated
2007-04-17
Date posted
2007-05-31
Date terminated
2008-05-05
Location
South Jordan, UT

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Related 510(k) clearances

RecordFirmDate
MERIT ADMINISTRATION SET (K915678)Merit Medical Systems, Inc.1992-07-30