FDA recall record

Medical Components, Inc dba MedComp 9.6F Plastic Dignity Mid-Sized CT Port w/Pre-Attached recall — FDA Z-1536-2017

The 9.6F port kits were packaged with the incorrect valved peelable introducer. The label states the kit contains a 10F valved peelable introducer. The…

Class IIclassification
Z-1536-2017official record ID
Mar 29, 2017report date

Recall record at a glance

Official recordZ-1536-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedical Components, Inc dba MedComp
Report dateMar 29, 2017
Recall initiation dateFeb 23, 2017
Quantity71 units
LocationHarleysville, PA, United States

Official product description

9.6F Plastic Dignity Mid-Sized CT Port w/Pre-Attached Silicone Catheter The CT Power Injectable Implantable Infusion Ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products, and for the withdrawal of blood samples. When used with a power injectable needle, the Power Injectable Implantable Infusion Port device is indicated for power injection of contrast media

Why the product was recalled

The 9.6F port kits were packaged with the incorrect valved peelable introducer. The label states the kit contains a 10F valved peelable introducer. The kit is packaged with a 9F valved peelable introducer. The port lumen will not fit through the introducer during the insertion procedure.

Distribution information

Worldwide Distribution to PR and Panama

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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