Medical device recalls Moderate risk

Waldemar Link GmbH & Co. KG (Mfg Site) recalls Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

Recall date
February 11, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1651-2026
FDA classification
Class II
Brand / firm
Waldemar Link GmbH & Co. KG (Mfg Site)
Sold / distributed
US distribution to states of: AL, AZ, FL, GA, IL, IN, KS, KY, LA, MI, NC, OH, OK, TX, VA

Why it was recalled

The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps described in the surgical technique are correct.

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

What was recalled

Embrace Drill Tower, Wedged (25mm); Item Number: 645-081/62;

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