PlainRecalls
FDA Devices Moderate Class II Terminated

OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.

Reported: December 23, 2020 Initiated: November 25, 2020 #Z-0623-2021

Product Description

OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.

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?
OSS Polyethylene Tibial Bushing, Item number 150476 - Product Usage: intended for use in limb salvage.. 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-0623-2021.