FDA recall record

CareFusion 303 MaxGuard Extension Set, Model No recall — FDA Z-1482-2017

CareFusion is recalling the MaxGuard Extension Set due to reports of leaks occurring with the 0.2 micron filter.

Class IIclassification
Z-1482-2017official record ID
Mar 22, 2017report date

Recall record at a glance

Official recordZ-1482-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCareFusion 303, Inc.
Report dateMar 22, 2017
Recall initiation dateFeb 20, 2017
Quantity12,850 units
LocationSan Diego, CA, United States

Official product description

MaxGuard Extension Set, Model No. ME2064, MP9009C, MP9209, MP9254C The MaxGuard extension sets are used to administer fluids from a container to a patient s vascular system through a needle or catheter inserted into the patient s artery or vein. The extension sets may incorporate components that aid in the prevention of accidental needle sticks. The set s components are commonly found on intravascular administration sets and extension sets

Why the product was recalled

CareFusion is recalling the MaxGuard Extension Set due to reports of leaks occurring with the 0.2 micron filter.

Distribution information

Nationwide Distribution

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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