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M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedu...

FDA Recall #Z-0622-2021 — Class II — November 25, 2020

Recall #Z-0622-2021 Date: November 25, 2020 Classification: Class II Status: Terminated

Product Description

M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.

Reason for Recall

Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.

Recalling Firm

Biomet, Inc. — Warsaw, IN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

7428

Distribution

Worldwide distribution. US nationwide, ARGENTINA, AUSTRALIA, Brazil, CANADA, CHILE, CHINA, COSTA RICA, EMEA, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, NEW ZEALAND, SINGAPORE, and TAIWAN

Code Information

Lot number 832990

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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