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FDA Medical Device Recalls (openFDA)

Merit Medical Systems, Inc.: Merit Medical Systems, Inc. Prelude Pro Sheath Introducer REF/CAT No.: PRO-6F-11-035 Prelude PRO SHEATH INTRODUCER 6F 11 cm to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries.

Recall number
Z-0519-2010
Recalling firm
Merit Medical Systems, Inc.
Product
Merit Medical Systems, Inc. Prelude Pro Sheath Introducer REF/CAT No.: PRO-6F-11-035 Prelude PRO SHEATH INTRODUCER 6F 11 cm to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries.
Status
Terminated
Initiated
2009-09-29
Posted
2009-12-14
Terminated
2009-12-15
Reason
Potential sterility breach caused by excessive shipment damage.
Root cause
Other
Action
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.
Quantity
5 Sheath Introducers
Distribution
US (AL, LA, MO, KY, TN, GA). No military, government or foreign distribution.
Lot, serial or model codes
Lot #F712835
510(k) numbers
["K050962"]
PMA numbers
not on file
Product code
DRE
Firm FEI
1721504
Firm city
South Jordan
Firm state
UT
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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