PlainRecalls
FDA Devices Low Class III Terminated

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.

Reported: March 18, 2020 Initiated: February 7, 2020 #Z-1470-2020

Product Description

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.

Reason for Recall

Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.

Details

Units Affected
55
Distribution
Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, IN, LA, MI, MN, MO, NC, NM, NY, PA, SC, and TX and countries of Italy, France, Germany, and Finland.
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.. Recalled by Integra LifeSciences Corp.. Units affected: 55.
Why was this product recalled?
Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 18, 2020. Severity: Low. Recall number: Z-1470-2020.