FDA recall Z-0920-2021

OMNIlife science Inc. · Class II · device

Product

SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup for total hip replacement procedures. Product Code: H6-25128

Reason for recall

Acetabular Liners have a higher than acceptable oxidation limit, potential for patients to experience a higher wear rate for acetabular liners and require a revision surgery

Distribution

AL, ID, MD, NY, OK

Key facts

Status
Terminated
Initiation date
2020-12-21
Report date
2021-02-03
Termination date
2021-06-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Raynham, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0920-2021