Stryker GmbH recalls Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S

Recall date

April 27, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2405-2018

FDA classification

Class II

Brand / firm

Stryker GmbH

Sold / distributed

The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA.

Why it was recalled

The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S