FDA Enforcement Class II Ongoing

LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2220/40

Recall: Z-1539-2023 · Reported May 10, 2023

Enforcement

Recall Number
Z-1539-2023
Event ID
92088
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Linkbio Corp.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
May 10, 2023
Initiation Date
March 21, 2023
Classification Date
May 4, 2023
Address
101 Round Hill Dr Ste 7, Rockaway, NJ, 07866-1214, United States

Description

LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, SMALL Item Number: 15-2220/40

Reason

Additional Label Warnings: Amendment / reinforcement of the Surgical Technique and future product training on the updated technique, due to early aseptic loosening or increased wear of the implant caused by suboptimal positioning of the implant or inadequate cementing technique leading to an unsatisfactory surgical result, and in the worst case, intervention or revision earlier than expected

Code Info

UDI-DI: 04026575429073 All lot numbers within expiration date

Distribution

NY, NV Foreign: Bulgaria, France, Italy, Norway, Poland, Sweden, Switzerland, Slovakia, Spain, United Kingdom, Germany, Austria, Argentina, Australia, China, India, Iraq, Jordan, Colombia, Mexico, Saudi Arabia, Ukraine, Vietnam, and Belarus

Quantity

5 units