M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.
Reported: December 23, 2020 Initiated: November 25, 2020 #Z-0622-2021
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.
Details
- Recalling Firm
- Biomet, Inc.
- Units Affected
- 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
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
M/H MODULAR STEM, Item number 13-104756 - Product Usage: intended for use in limb salvage procedures.. Recalled by Biomet, Inc.. Units affected: 7428.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 23, 2020. Severity: Moderate. Recall number: Z-0622-2021.
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