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Serious recall: Injury is possible or has been reported. Take action promptly.

LINK BIO CORP 2024-07-31 Health serious FDA
Health · FDA · Recall #FDA-Z-2445-2024

LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00 Recall

Issued July 31, 2024 · LINK BIO CORP

In July 2024, LINK BIO CORP recalled the LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The markings on two arms of the instrument were mixed up because the triangular Patella Sizing Template was inserted upside down into the laser marking process.

What you should do

  1. 1 Stop using LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00 right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact LINK BIO CORP to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
LINK BIO CORP
Category
Health
Recall date
July 31, 2024
Units affected
Not reported
Sold at
US Nationwide distribution in the states of FL, GA, KS, OH, WI.
Recall number
FDA-Z-2445-2024
Made in
United States
Issuing agency
FDA

In context

  • LINK BIO CORP has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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