Lower riskMedical device recall · FDA · Published July 27, 2020
MedComp 15.SF X 24CM Titan HD Catheter Recall: Incorrect Valve Size Risk
MedComp recalls 15.SF X 24CM Titan HD catheters with incorrect 15F valve instead of 16F. This mismatch may cause complications during medical procedures. Affected units have specific lot numbers and expiration dates.
Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
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Contact the company
📍Recalling firmMedical Components, Inc dba MedComp1499 Delp Dr · Harleysville, PA 19438-2936
✎ GovInfoNow plain-language explainer
MedComp is recalling a specific type of medical catheter because it was shipped with the wrong valve size (15F instead of 16F). Using this incorrect valve could lead to complications during medical procedures. This recall affects catheters with the reference number THD155024. Read more at govinfonow.com/recall/64631-medcomp-15-sf-x-24cm-titan-hd-catheter-recall-incorrect.
“MedComp 15.SF X 24CM Titan HD Catheter Recall: Incorrect Valve Size Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64631-medcomp-15-sf-x-24cm-titan-hd-catheter-recall-incorrect. Based on FDA recall #Z-2940-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2940-2020%22&limit=1).
The FDA announced on July 27, 2020, that Medical Components, Inc. dba MedComp voluntarily recalled the Medcomp 15.SF X 24CM Titan HD CATHETER due to packaging errors. The hazard involves kits containing an incorrect size valve peelable introducer.
How to tell if you have it
Brand: MedComp
Product: Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP)
Reference: THD155024
Lot #: MPCT670
UDI: 884908129304
Expiration Date: 12/20/2020
The hazard
According to the FDA, the kits were packaged with a 15F valve peelable introducer instead of the correct 16F size. The recall involves 132 units distributed in AZ, CA, FL, GA, NC, ND, NJ, NY, OH, PA, VA, and WA.
Context
GovInfoNow's records show Medical Components, Inc. dba MedComp has 7 other recalls on record since November 22, 2017. Other recent recalls of similar products include MedComp Power Injectable CT Port Kits Recalled (January 13, 2021) and MedComp 14F SLX Catheter Kits Have Wrong Introducer Type - Recall (March 13, 2019). Additional similar product recalls include Medline Intubation Tray Recall (December 24, 2025), Medline Medical Procedure Kits Recall (May 4, 2026), and Medline Medical Procedure Kits: Catheter Issues Recalled (May 4, 2026).
How to tell if you have this one
Check for the reference number THD155024 on the catheter packaging. The catheter has a 15.SF X 24CM Titan HD size with a 19cm cuff from the tip. Lot numbers starting with MPCT670 and expiration date 12/20/2020 are affected.
Brand
MedComp
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the catheter's reference number, lot number, and expiration date to confirm if it matches the recalled items.
Where it went and when
Where it was distributed
Distributed in 12 states.
Listed by the agency
Not listed
FDA distribution: “AZ, CA. FL. GA, NC, ND, NJ, NY, OH, PA, VA, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Florida, Georgia, New Jersey, New York, North Carolina, North Dakota, Ohio, Pennsylvania, Virginia, Washington.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
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-2940-2020 (July 27, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2940-2020 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.