FDA recall record

Medical Components, Inc dba MedComp Medcomp 15.SF X 24CM Titan HD CATHETER recall — FDA Z-2940-2020

Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer

Class IIclassification
Z-2940-2020official record ID
Sep 16, 2020report date

Recall record at a glance

Official recordZ-2940-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedical Components, Inc dba MedComp
Report dateSep 16, 2020
Recall initiation dateJul 27, 2020
Quantity132 eaches
LocationHarleysville, PA, United States

Official product description

Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024

Why the product was recalled

Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer

Distribution information

AZ, CA. FL. GA, NC, ND, NJ, NY, OH, PA, VA, WA

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

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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