14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061425 Product Usage: An aid for introducing a hemodialysis catheter
FDA Recall Z-2217-2019 · Posted None
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Recalling FirmMedical Components, Inc dba MedComp
Recall StatusTerminated
Product CodeLFJ
Date Initiated2019-03-13
Date Terminated2024-03-05
Product Quantity6830
Reason for Recall
Tray label indicates the kits are packaged with a 15F "valved" peelable introducer, but the kits contain a 15F "non-valved" peelable introducer.
Firm Action
On March 13, 2019, the firm notified customers via Urgent Medical Device Recall letter. Customers were
informed that the kits contain a 15F "non-valved" peelable introducer despite the label indicating that the kit is
packaged with a "valved" introducer. Customers were asked to do the following: 1. Immediately examine your
inventory and quarantine product subject to recall. 2. If you have further distributed this product, please
identify your customers and immediately notify them of the recall. 3. Contact your Medical Components, Inc.
customer service representative for a Returned Goods Authorization (RGA) number if you have product to
return. The phone number to call is 215-256-4201. 4.Complete and return the Medical Device Recall Return
Response Form. The form can be returned by fax (215-256-9191) or email ([email protected]).
Contact Information for questions: Monday through Friday, 8:00 AM to 4:00 PM, Eastern Standard Time.
Phone: 215-256-4201; Email: [email protected]
Root Cause
Labeling Change Control
Distribution Pattern
US Nationwide Distribution CA FL GA IN KY LA MA MI MO MS NJ NY OH OK PA SC TN TX VA WV.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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