FDAClass IIAugust 17, 2016

Integra External Fixation System Slotted Post - Small recall

Integra External Fixation System Slotted Post - Small Catalogue #12224228; Integra External Fixation System Slotted Post Large Catalogue #12224229

Why was Integra External Fixation System Slotted Post - Small recalled?

Through the investigation of reported complaints Integra verified that there have been instances where the Universal Wire Fixation Bolts the Slotted Post broke during use at the surgical site.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Lot # QJ0139, QJ0148, QJ0140, QJ0149, QJ0287

Product
Integra External Fixation System Slotted Post - Small Catalogue #12224228; Integra External Fixation System Slotted Post Large Catalogue #12224229
Recalling firm
Integra LifeSciences Corp.
Quantity
111 units
Distribution
US Distribution to the states of : FL, VA, OK, CO, DC and IN.
Recall date
August 17, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls