PlainRecalls
FDA Devices Moderate Class II Terminated

Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.

Reported: February 25, 2015 Initiated: January 9, 2015 #Z-1123-2015

Product Description

Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.

Reason for Recall

Biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging with the two.

Details

Recalling Firm
Biomet, Inc.
Units Affected
17
Distribution
Distributed in the states of VA and TX and the country of Japan.
Location
Warsaw, IN

Frequently Asked Questions

What product was recalled?
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.. Recalled by Biomet, Inc.. Units affected: 17.
Why was this product recalled?
Biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging with the two.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 25, 2015. Severity: Moderate. Recall number: Z-1123-2015.