FDA recall record

Integra Cranial Access Kit, Model Number HITHSP10, Rx Only recall — FDA Z-0551-2014

Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10 Cranial Access Kits due to identified labeling discrepancies. kit contains…

Class IIclassification
Z-0551-2014official record ID
Jan 1, 2014report date

Recall record at a glance

Official recordZ-0551-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIntegra LifeSciences Corp. d.b.a. Integra Pain Management
Report dateJan 1, 2014
Recall initiation dateNov 26, 2013
Quantity731
LocationSalt Lake City, UT, United States

Official product description

Integra Cranial Access Kit, Model Number HITHSP10, Rx Only. Integra Cranial Access Kits (CRAK) allows for burr hole access to the subarachnoid space or the lateral ventricles of the brain. The kit is intended to be used with an external drainage and monitoring system in selected patients to reduce intracranial pressure (ICP), to monitor CSF, to provide temporary drainage of Cerebrospinal Fluid (CSF), and to monitor ICP. These kits contain all components and accessories required for burr hole access into the cranium.

Why the product was recalled

Integra LifeSciences is voluntarily recalling any unexpired lots of HITHSP10 Cranial Access Kits due to identified labeling discrepancies. kit contains DuraPrep and Monocryl sutures whose labeling does not align with the intended use and labeling of the Cranial Access Kit.

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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Related recall records

Other records from the same recalling company are shown first when available.

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Integra LifeSciences has been notified of a medical device recall by Adaptive Surgical, LLC involving their Riverlon" Nylon 3-0 Sutures that are packaged in Integras Cranial Access Kits.…

Class IIFDA: TerminatedIntegra LifeSciences Corp. d.b.a. Integra Pain…