Medical Components, Inc dba MedComp recalls
Every recall we track for Medical Components, Inc dba MedComp — 29 in all, from 2017–2021 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Medical Components, Inc dba MedComp peaked in 2018 (22); 29 since 2017. 7% rated “stop using now”.
All FDA recall records for Medical Components, Inc dba MedComp since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 2 | 13 | 7 | 0 | 22 |
| 2019 | 0 | 0 | 4 | 0 | 4 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Medical Components, Inc dba MedComp product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medical Components, Inc dba MedComp recalls
8 shown- Use cautionMedical device
Medical Components, Inc dba MedComp recalls Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated
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.
MedCompJan 13, 2021 - Lower riskMedical device
Medical Components, Inc dba MedComp recalls Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
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.
MedCompJul 27, 2020 - Lower riskMedical device
Medical Components, Inc dba MedComp recalls 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061424 Product Usage: An aid for
MedComp recalls 14F x 24CM SLX Double Lumen Hemodialysis catheter kits that contain a non-valved introducer instead of the labeled valved type. This could lead to complications during dialysis procedures.
MedCompMar 13, 2019 - Lower riskMedical device
Medical Components, Inc dba MedComp recalls 14F SLX Double Lumen Full Tray Hemodialysis catheter insertion kits, Item No. MC061422
MedComp recalls 14F SLX Double Lumen Hemodialysis catheter kits that contain non-valved introducers instead of valved ones, which could cause complications during dialysis.
MedCompMar 13, 2019 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls C3 Wave App, v. 2.0.5
MedComp recalls C3 Wave App v. 2.0.5 due to ECG waves not appearing after iOS 12 update, risking incorrect PICC placement.
MedCompOct 1, 2018 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET; T94C T94M T96M T98M
MedComp recalls SOFT-LINE DUO-FLOW double lumen catheter sets (T94C, T9: 150 characters
MedCompJul 12, 2018 - Use cautionMedical device
Medical Components, Inc dba MedComp recalls 12F Tesio CATHETER SET (CUFF 32CM FROM TIP), REF MCTC1247SD, UDI 884908027266 Product Usage: The Medcomp Repair Kit is
MedComp recalls 12F Tesio Catheter Set (REF MCTC1247SD) due to potential connection failures causing blood loss or air emboli. Affected units have specific lot numbers and UDI.
MedCompFeb 23, 2018 - Lower riskMedical device
Medical Components, Inc dba MedComp recalls 8F Plastic Dignity¿ Low Profile CT Port W/Pre-Attached ChronoFlex¿ Polyurethane Catheter
MedComp recalls 8F Plastic Dignity Low Profile CT Port kits with incorrect unmarked guidewires. These kits may cause complications during medical procedures. Affected kits have specific lot numbers and expiration dates.
MedCompNov 22, 2017
Medical Components, Inc dba MedComp recall questions
How many recalls has Medical Components, Inc dba MedComp had?
29 recalls from Medical Components, Inc dba MedComp are on record with U.S. safety agencies, from 2017–2021.
What is the most recent Medical Components, Inc dba MedComp recall?
Medical Components, Inc dba MedComp recalls Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated, dated Jan 13, 2021. Every Medical Components, Inc dba MedComp recall is listed on this page, newest first.
What should I do if I have a recalled Medical Components, Inc dba MedComp product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medical Components, Inc dba MedComp recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.