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MEDCOMP GEN III POWER INJECTABLE PORTMEDCOMP GEN III POWER INJECTABLE PORT

Medical Components, Inc. · Model MRCTI9680S · UDI-DI 00884908084702

LJT Prescription

510(k) clearances

22,474

Adverse events (405 deaths)

141

Recalls

Facilities

Description

9.6F PLASTIC DIGNITY® MID-SIZED CT PORTMID-SIZED CT PO W/SILICONE FILLED SUTUREW/SILICO HOLES W/PRE-ATTACHEDHOLES W/PRE- SILICONE CATHETERSILICONE CATHET

Recalls

Date	Firm	Reason
2026-04-21	ARROW INTERNATIONAL, LLC	Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo
2025-07-21	B.Braun Medical S.A.S.	The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
2025-02-13	Smiths Medical ASD, Inc.	The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.