FDA recall record

Arrow International Radial Artery Catheterization Kit with Sharps Safety Features Permits recall — FDA Z-2741-2016

Shipping carton labeling error.

Class IIclassification
Z-2741-2016official record ID
Sep 14, 2016report date

Recall record at a glance

Official recordZ-2741-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArrow International Inc.
Report dateSep 14, 2016
Recall initiation dateAug 8, 2016
Quantity690 kits
LocationReading, PA, United States

Official product description

Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.

Why the product was recalled

Shipping carton labeling error.

Distribution information

Nationwide Distribution to OH, IN, TN, NC, and KY.

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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