RecallDepth

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

This recall has been terminated (originally issued December 21, 2020).

Company
Omnilife Science Inc.
Recall Initiated
December 21, 2020
Terminated
June 10, 2021
Recall Number
Z-0920-2021
Quantity
3 units
Firm Location
Raynham, MA
Official Source
View on FDA website ↗

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

Lot / Code Info

Lot Number: 28413

Root Cause

Under Investigation by firm

Action Taken

Omni Life Initial communication was sent by email via a quarantine form on 12/09/2020. On 12/22/20 a notification packet detailing parameters of recall sent via email and overnight mail. Acknowledgement of receipt is requested. Actions to be taken by the Customer/User " Immediately quarantine lots 28413, 28624 and 28572 " Return Product to OMNI at 480 Paramount Drive, Raynham MA 02767 " This advisory notice only includes the lots identified above. It does not affect other lots. You must acknowledge this notice by returning the attached Acknowledgement and Receipt Form by FAX to 508-819-3390 or my email to Omni-cs@coringroup.com.

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