FDA recall record

The Metrix Company SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF recall — FDA Z-3240-2017

The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and…

Class IIclassification
Z-3240-2017official record ID
Oct 11, 2017report date

Recall record at a glance

Official recordZ-3240-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThe Metrix Company
Report dateOct 11, 2017
Recall initiation dateSep 13, 2017
Quantity50 cases of 200 units
LocationDubuque, IA, United States

Official product description

SECURE(R) 100mL EMPTY VINYL CONTAINER With 2 Ports - (5 Boxes of 40), REF 58719, STERILE R,

Why the product was recalled

The hot stamp label on the bag incorrectly states the material of the vinyl (bag) container. The bags are correctly made with PVC material, as ordered and as labeled on the inner and outer boxes.

Distribution information

AZ, MA, IL, FL

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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