FDA recall record

Aesculap ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral recall — FDA Z-1806-2013

Aesculap Implant Systems, LLC initiated a recall of the Aesculap Prospace PEEK 5 degree Implant - 8 x 8.5 x 22 mm (SN038P) because the device is…

Class IIclassification
Z-1806-2013official record ID
Jul 31, 2013report date

Recall record at a glance

Official recordZ-1806-2013
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAesculap, Inc.
Report dateJul 31, 2013
Recall initiation dateJun 18, 2013
Quantity9
LocationCenter Valley, PA, United States

Official product description

ProSpace Peek Implant 5 degree x 8.5 x 22 mm The device is intended for vertebral body replacement or intervertebral body fusion to aid in the surgical correction or stabilization of the spine. The Aesculap PEEK Spinal Implant System is indicated for use in the thoracolumbar spine (T1 to L5) for partial or total replacement of a collapsed, damaged, or unstable vertebral body due to tumor or trauma to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body.

Why the product was recalled

Aesculap Implant Systems, LLC initiated a recall of the Aesculap Prospace PEEK 5 degree Implant - 8 x 8.5 x 22 mm (SN038P) because the device is incorrectly etched with an 8 degree lordosis instead of a 5 degree lordosis. The device is labeled correctly, only the etching of the implant may be incorrect.

Distribution information

US Distribution including the states of NV and MI

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: E-Mail.

What to do next

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About this record

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