FDAClass IIDecember 13, 2023

Combo Kit Consists OF 10-110/INS-4500/INS-7040- For recall: Sterility Concern

Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: 31004

Why was Combo Kit Consists OF 10-110/INS-4500/INS-7040- For recalled?

Defect in the outer packaging of the Cranial Access Kits. can cause the packaging to split without any additional forces outside compromising the sterility of the device

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: 10381780178095 Lot Number/Exp. Date: 6926457 31-May-24

Product
Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: 31004
Recalling firm
Integra LifeSciences Corp.
Quantity
1 unit
Distribution
Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Belgium, Canada, Chile, France, Ireland, Israel, South Africa, United Kingdom.
Recall date
December 13, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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