Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
FDA Recall Z-2483-2015 · Posted 2015-08-29
Recalling FirmBiomet, Inc.
Recall StatusTerminated
Product CodeLPH
Date Initiated2015-07-28
Date Terminated2016-05-17
Product Quantity5
Reason for Recall
The device was assembled without screw hole plugs.
Firm Action
Zimmer Biomet issued notices on July 28, 2015, via FedEx overnight mail and e-mail to customers. Customers were asked to return response forms and recalled devices to Zimmer Biomet. Customers with questions may call Seth Pixton, Field Action Specialist, at 574-372-1570, Monday through Friday from 8:00 am to 5:00 pm, or e-mail at: [email protected].
Root Cause
Under Investigation by firm
Distribution Pattern
Distributed in Canada and Japan.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.