14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422
FDA Recall Z-1149-2019 · 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
Finished device change control
Distribution Pattern
Distributed to accounts in 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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