Use cautionMedical device recall · FDA · Published January 13, 2021
MedComp Power Injectable CT Port Kits Recalled: Incorrect Port Size May Prolong Surgery
MedComp recalls Power Injectable CT Port insertion kits with incorrect 6.6F port instead of 5F. This may cause prolonged surgery and increased surgical risks. Affected kits have catalog number MRDP50AXS.
The 5F Dignity CT Port kits were packaged with the incorrect size port. The kits include a 6.6F port instead of the correct 5F port. The inability to connect the catheter lumen to the port stem because of the incorrect size may not be noted until well into the procedure, after the catheter lumen is placed in the vessel. An alternate port will need to be obtained prolonging the procedure. A prolonged insertion procedure increases any risk associated with a surgical procedure.
Take action
Contact the company
📍Recalling firmMedical Components, Inc dba MedComp1499 Delp Dr · Harleysville, PA 19438-2936
“MedComp Power Injectable CT Port Kits Recalled: Incorrect Port Size May Prolong Surgery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63428-medcomp-power-injectable-ct-port-kits-recalled-incorrect-port-size. Based on FDA recall #Z-1184-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1184-2021%22&limit=1).
The FDA announced on Jan. 13, 2021, that Medical Components, Inc. dba MedComp is recalling Power Injectable CT Port insertion kits due to packaging errors. The hazard involves incorrect port sizes that may prolong surgical procedures.
How to tell if you have it
Brand: MedComp
Product: Power Injectable CT Port insertion kits
Catalog Number: MRDP50AXS
Lot Numbers: MPDX180, MPCY660
UDI Number: 884908149753
The hazard
According to the FDA, the 5F Dignity CT Port kits were packaged with a 6.6F port instead of the correct 5F size. This mismatch may prevent connection of the catheter lumen to the port stem, potentially going unnoticed until after placement in the vessel. An alternate port will need to be obtained, prolonging the procedure and increasing risks associated with the surgery.
Context
GovInfoNow's records show Medical Components, Inc. dba MedComp has issued seven other recalls since Nov. 22, 2017. Previous issues included incorrect valve sizes in Titan HD Catheter kits recalled on July 27, 2020, and wrong introducer types in Hemodialysis Catheter Kits recalled on March 13, 2019. Other recent recalls of similar products include Medline Medical Procedure Kits Recall: Catheter Issues (May 4, 2026) and Medline Medical Procedure Kits: Catheter Issues Recalled (May 4, 2026).
How to tell if you have this one
Check for catalog number MRDP50AXS on the kit packaging. Kits sold with lot numbers MPCY660 or MPDX180 are affected.
Brand
MedComp
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Port Size
Verify the port size on the kit is 5F; if it's 6.6F, the kit is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 12 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of CA, DC, GA, IL, IN, MA, MI, NJ, NM, NY, OH, PA, TX. Updated 3/11/2021” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, District of Columbia, Georgia, Illinois, Indiana, Massachusetts, Michigan, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Texas.
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1184-2021 (January 13, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1184-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.