RecallDepth

Excella II Polyaxial Pedicle Screw used as a pedicle screw system in skeletally mature patients, is intended to provide immobilization and stabilization of spinal segments, as an adjunct to fusion, in treatment of the following acute and chronic deformities of the thoracic, lumbar, and sacral spine:

This recall has been terminated (originally issued January 8, 2018).

Company
Innovasis, Inc
Recall Initiated
January 8, 2018
Terminated
February 27, 2018
Recall Number
Z-0644-2018
Quantity
1,010 parts
Firm Location
Salt Lake City, UT
Official Source
View on FDA website ↗

Reason for Recall

Nine lots of 8.5 mm Polyaxial Pedicle Screws are at risk of breakage.

Distribution

United States

Lot / Code Info

Catalog/Part No.: E2S8530, E2S8535, E2S8540, E2S8545, E2S8550, E2S8555, E2S8560 with Lot Number: 1101 and Catalog/Part No.: E28540, E28545 with Lot Number: 1201. Each of these parts is engraved with part number and lot number.

Root Cause

Nonconforming Material/Component

Action Taken

The distributors were notified of the recall on 1/8/2018 via email with an attached pdf. They are also being asked to confirm or deny the quantities showing in inventory via a Product Removal Form sent in the same email.

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