FDA Device Intelligence
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Catheter, Subclavian

FDA product code LFJ · Class 2 · Gastroenterology, Urology

170
Registered devices
2,170
Adverse events
6
Recalls
65
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-04-21ARROW INTERNATIONAL, LLCLidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality iss
2019-03-13Medical Components, Inc dba MedCompTray label indicates the kits are packaged with a 15F "valved" peelable introducer, but the kits contain a 15F "non-valved" peelable introducer.
2019-03-13Medical Components, Inc dba MedCompTray label indicates the kits are packaged with a 15F "valved" peelable introducer, but the kits contain a 15F "non-valved" peelable introducer.
2019-03-13Medical Components, Inc dba MedCompTray label indicates the kits are packaged with a 15F "valved" peelable introducer, but the kits contain a 15F "non-valved" peelable introducer.
2019-03-13Medical Components, Inc dba MedCompTray label indicates the kits are packaged with a 15F "valved" peelable introducer, but the kits contain a 15F "non-valved" peelable introducer.
2015-01-21Medical Components, Inc dba MedCompDrug products contained within the kits may have been rendered ineffective by a duplicate sterilization process. The kits include one or more of the following

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.