FDA Device Recalls

Recalls /

#85864

Product

Merit Medical Systems, Inc. Prelude Short Sheath Introducer REF/CAT No.: PSS-6F-4-018MT Prelude SHORT SHEATH INTRODUCER 21G 6F-SMT 4 cm to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries.

FDA product code
DYBIntroducer, Catheter
Device class
Class 2
Medical specialty
Cardiovascular
510(k) numbers
K082063
Affected lot / code info
Lot #: F696474

Why it was recalled

Potential sterility breach caused by excessive shipment damage.

Root cause (FDA determination)

Other

Action the firm took

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.

Recalling firm

Firm
Merit Medical Systems, Inc.
Address
1600 Merit Pkwy South, Jordan, Utah 84095

Distribution

Distribution pattern
US (AL, LA, MO, KY, TN, GA). No military, government or foreign distribution.

Timeline

Recall initiated
2009-09-29
Posted by FDA
2009-12-14
Terminated
2009-12-15
Status

Source: openFDA Device Recall endpoint. Recall record ID #85864. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.