RecallDepth

LINK SymphoKnee System L-Shaped Femoral Augment, Medial-Right/Lateral-Left, Sz 5-6 Tilastan, cemented. Intended for primary and revision total knee replacement. Item Number: 880-325/13

Company
Linkbio Corp.
Recall Initiated
April 25, 2023
Posted
June 1, 2023
Recall Number
Z-1674-2023
Quantity
11 units
Firm Location
Rockaway, NJ

Reason for Recall

Contains the incorrect implant in the packaging. The packaging incorrectly contains the opposite side of the implant (Lateral-Right/Medial-Left instead of Medial-Right/Lateral-Left).

Distribution

US Nationwide Distribution - AL, GA, IL, IN, LA, NV, TX

Lot / Code Info

UDI-DI : 04026575258123 Lot Number: 1910003

Root Cause

Under Investigation by firm

Action Taken

LinkBio Corp. issued Urgent Medical Device Recall on 4/25/23 via email to Distributors. Letter states reason for recall, health risk and action to take: Please respond using the attached Distributor Reply form to indicate your understanding of this Device Recall and of the need to return the affected product. Pre-paid shipping labels will be provided once the Distributor Reply Form is returned. Please return the product as soon as possible to the following address: LinkBio Corporation 69 King St Dover, NJ 07801. Please contact LinkBio at 973-625-1333 or complaints@linkbio.com for any questions.

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