FDAFebruary 18, 2019device

DS-0024 QUICK START DISTRACTION SCREW 14MM 5/BOX STERILE - Product Usage: These products are intended to be used by trained surgeons and are designed for use with TSI distractors and screwdrivers.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The items identified for recall are labeled as sterile. However, the manufacturer has found that product packaging for the lots listed above may be damaged, potentially exposing the product to non sterile conditions. This situation presents a risk of infection to patients.

What to do

FDA enforcement status: Terminated

Brands named

tedan surgical innovationstedantedan surgical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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