FDA recall record

ZOLL Circulation 7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen recall — FDA Z-0477-2015

After aquisition of assets of CoAxia, Zoll discovered that one lot of NeuroFlo Catheters was manufactured by another firm and an HDE supplement listing as…

Class IIclassification
Z-0477-2015official record ID
Dec 3, 2014report date

Recall record at a glance

Official recordZ-0477-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmZOLL Circulation, Inc.
Report dateDec 3, 2014
Recall initiation dateApr 1, 2014
Quantity1 device
LocationSan Jose, CA, United States

Official product description

7F NeuroFlo Catheter, Model 1027 The NeuroFlo Catheter is a multi-lumen device with two balloons mounted near the distal tip for the treatment of cerebral ischemia resulting from symptomatic vasospasm following aneurysmal subarachnoid hemorrhage. The NeuroFlo Catheter is under Humanitarian Device Exemption and not commercially released under a premarket notification or premarket approval.

Why the product was recalled

After aquisition of assets of CoAxia, Zoll discovered that one lot of NeuroFlo Catheters was manufactured by another firm and an HDE supplement listing as the owner of the product was not filed.

Distribution information

One location in NC

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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