FDA recall record

Vygon MFG, Inc., dba/ Churchill Medical Systems 4Fr x 20cm Single Lumen CT Midline Basic recall — FDA Z-0585-2020

Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.

Class IIclassification
Z-0585-2020official record ID
Dec 4, 2019report date

Recall record at a glance

Official recordZ-0585-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmVygon MFG, Inc., dba/ Churchill Medical Systems, Inc.
Report dateDec 4, 2019
Recall initiation dateSep 24, 2019
Quantity75
LocationDover, NH, United States

Official product description

4Fr x 20cm Single Lumen CT Midline Basic Tray, Product Code: VYML4S1001

Why the product was recalled

Potential that 3Fr size catheter placed in the catheter tray instead of 4Fr for the 4Fr x 20cm Single Lumen CT Midline Basic Tray.

Distribution information

One Customer Located in TN

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: not stated.

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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Class IIFDA: TerminatedVygon MFG, Inc., dba/ Churchill Medical Systems, Inc.