PlainRecalls
FDA Devices Moderate Class II Terminated

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.

Reported: September 9, 2015 Initiated: July 28, 2015 #Z-2483-2015

Product Description

Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.

Reason for Recall

The device was assembled without screw hole plugs.

Details

Recalling Firm
Biomet, Inc.
Units Affected
5
Distribution
Distributed in Canada and Japan.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.. Recalled by Biomet, Inc.. Units affected: 5.
Why was this product recalled?
The device was assembled without screw hole plugs.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 9, 2015. Severity: Moderate. Recall number: Z-2483-2015.