PlainRecalls
FDA Devices Moderate Class II Terminated

Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 13, Femoral Stem, Catalog Number 160-00-13; For use in primary total hip arthroplasty.

Reported: June 8, 2016 Initiated: April 12, 2016 #Z-1902-2016

Product Description

Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 13, Femoral Stem, Catalog Number 160-00-13; For use in primary total hip arthroplasty.

Reason for Recall

Devices were inadvertently sent to packaging and finished goods prior to the PMA site-change supplement approval.

Details

Recalling Firm
Exactech, Inc.
Units Affected
4 devices.
Distribution
Distributed in FL, NJ, NY, OH, OK, RI, TN, VA and HI.
Location
Gainesville, FL

Frequently Asked Questions

What product was recalled?
Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 13, Femoral Stem, Catalog Number 160-00-13; For use in primary total hip arthroplasty.. Recalled by Exactech, Inc.. Units affected: 4 devices..
Why was this product recalled?
Devices were inadvertently sent to packaging and finished goods prior to the PMA site-change supplement approval.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 8, 2016. Severity: Moderate. Recall number: Z-1902-2016.