United StatesLinkBio CORE Workstation, a component of the CORE Shoulder System (Product Code 87-9136, UDI‑DI 00810022403099; all serial numbers affected), is being recalled. The device may display an incorrect “Planning Date” when viewing cases on the “Start Case” menu screen. The recall covers five units distributed in Alabama, Florida, and Kansas in the United States.
What's being recalled
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
Recalling firm: Linkbio Corp., Rockaway, NJ, United States.
How to identify it
Product Code: 87-9136. UDI-DI: 00810022403099. All serial numbers of the CORE Workstation are affected.
The hazard
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of Alabama, Florida, and Kansas.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)